esv3593502

Organism: Homo sapiens

Study:estd214 (1000 Genomes Consortium Phase 3)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1,244
Validation:Not tested
Clinical Assertions: No
Region Size:16,737

Publication(s):1000 Genomes Project Consortium et al. 2015

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 554 SVs from 64 studies. See in: genome view

Remapped(Score: Perfect):179,199,556-179,218,292

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3593502	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
esv3593502	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000002.11	Chr2	180,065,283 (-1000, +500)	180,082,019 (-500, +1000)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv10779439	deletion	SAMN00004625	Sequencing	Read depth and paired-end mapping	Heterozygous	2,591
essv10779440	deletion	SAMN00004626	Sequencing	Read depth and paired-end mapping	Heterozygous	2,931
essv10779441	deletion	SAMN00004629	Sequencing	Read depth and paired-end mapping	Heterozygous	2,200
essv10779442	deletion	SAMN00004634	Sequencing	Read depth and paired-end mapping	Heterozygous	2,737
essv10779443	deletion	SAMN00004637	Sequencing	Read depth and paired-end mapping	Heterozygous	2,609
essv10779444	deletion	SAMN00004638	Sequencing	Read depth and paired-end mapping	Heterozygous	2,504
essv10779445	deletion	SAMN00006337	Sequencing	Read depth and paired-end mapping	Heterozygous	2,882
essv10779446	deletion	SAMN00006338	Sequencing	Read depth and paired-end mapping	Heterozygous	2,748
essv10779447	deletion	SAMN00006341	Sequencing	Read depth and paired-end mapping	Homozygous	2,683
essv10779448	deletion	SAMN00006344	Sequencing	Read depth and paired-end mapping	Heterozygous	2,768
essv10779449	deletion	SAMN00004645	Sequencing	Read depth and paired-end mapping	Heterozygous	2,148
essv10779450	deletion	SAMN00004646	Sequencing	Read depth and paired-end mapping	Heterozygous	2,568
essv10779451	deletion	SAMN00004647	Sequencing	Read depth and paired-end mapping	Heterozygous	2,660
essv10779452	deletion	SAMN00004650	Sequencing	Read depth and paired-end mapping	Heterozygous	2,682
essv10779453	deletion	SAMN00004651	Sequencing	Read depth and paired-end mapping	Heterozygous	2,831
essv10779454	deletion	SAMN00004655	Sequencing	Read depth and paired-end mapping	Heterozygous	2,454
essv10779455	deletion	SAMN00004657	Sequencing	Read depth and paired-end mapping	Heterozygous	2,763
essv10779456	deletion	SAMN00004659	Sequencing	Read depth and paired-end mapping	Homozygous	2,876
essv10779457	deletion	SAMN00004661	Sequencing	Read depth and paired-end mapping	Heterozygous	2,731
essv10779458	deletion	SAMN00004663	Sequencing	Read depth and paired-end mapping	Heterozygous	2,670
essv10779459	deletion	SAMN00004664	Sequencing	Read depth and paired-end mapping	Heterozygous	2,739
essv10779460	deletion	SAMN00004666	Sequencing	Read depth and paired-end mapping	Heterozygous	2,758
essv10779461	deletion	SAMN00006345	Sequencing	Read depth and paired-end mapping	Heterozygous	2,777
essv10779462	deletion	SAMN00004676	Sequencing	Read depth and paired-end mapping	Heterozygous	2,580
essv10779463	deletion	SAMN00016965	Sequencing	Read depth and paired-end mapping	Heterozygous	2,566
essv10779464	deletion	SAMN00016968	Sequencing	Read depth and paired-end mapping	Heterozygous	2,820
essv10779465	deletion	SAMN00016969	Sequencing	Read depth and paired-end mapping	Heterozygous	2,443
essv10779466	deletion	SAMN00016970	Sequencing	Read depth and paired-end mapping	Heterozygous	2,824
essv10779467	deletion	SAMN00016973	Sequencing	Read depth and paired-end mapping	Heterozygous	2,813
essv10779468	deletion	SAMN00016979	Sequencing	Read depth and paired-end mapping	Heterozygous	2,879
essv10779469	deletion	SAMN00006347	Sequencing	Read depth and paired-end mapping	Heterozygous	2,456
essv10779470	deletion	SAMN00004677	Sequencing	Read depth and paired-end mapping	Heterozygous	2,238
essv10779471	deletion	SAMN00004679	Sequencing	Read depth and paired-end mapping	Homozygous	2,446
essv10779472	deletion	SAMN00006348	Sequencing	Read depth and paired-end mapping	Heterozygous	2,664
essv10779473	deletion	SAMN00006350	Sequencing	Read depth and paired-end mapping	Heterozygous	2,652
essv10779474	deletion	SAMN00004681	Sequencing	Read depth and paired-end mapping	Heterozygous	2,727
essv10779475	deletion	SAMN00006353	Sequencing	Read depth and paired-end mapping	Homozygous	2,837
essv10779476	deletion	SAMN00006354	Sequencing	Read depth and paired-end mapping	Heterozygous	2,703
essv10779477	deletion	SAMN00009091	Sequencing	Read depth and paired-end mapping	Heterozygous	2,832
essv10779478	deletion	SAMN00004682	Sequencing	Read depth and paired-end mapping	Heterozygous	2,758
essv10779479	deletion	SAMN00006364	Sequencing	Read depth and paired-end mapping	Heterozygous	2,776
essv10779480	deletion	SAMN00006365	Sequencing	Read depth and paired-end mapping	Heterozygous	2,690
essv10779481	deletion	SAMN00006366	Sequencing	Read depth and paired-end mapping	Heterozygous	2,730
essv10779482	deletion	SAMN00006367	Sequencing	Read depth and paired-end mapping	Homozygous	2,481
essv10779483	deletion	SAMN00006368	Sequencing	Read depth and paired-end mapping	Heterozygous	2,552
essv10779484	deletion	SAMN00006372	Sequencing	Read depth and paired-end mapping	Heterozygous	2,697
essv10779485	deletion	SAMN00006373	Sequencing	Read depth and paired-end mapping	Heterozygous	2,538
essv10779486	deletion	SAMN00006376	Sequencing	Read depth and paired-end mapping	Heterozygous	2,448
essv10779487	deletion	SAMN00006377	Sequencing	Read depth and paired-end mapping	Homozygous	2,795
essv10779488	deletion	SAMN00009094	Sequencing	Read depth and paired-end mapping	Heterozygous	2,610
essv10779489	deletion	SAMN00009095	Sequencing	Read depth and paired-end mapping	Heterozygous	2,620
essv10779490	deletion	SAMN00009099	Sequencing	Read depth and paired-end mapping	Heterozygous	2,678
essv10779491	deletion	SAMN01761612	Sequencing	Read depth and paired-end mapping	Heterozygous	2,789
essv10779492	deletion	SAMN01761624	Sequencing	Read depth and paired-end mapping	Heterozygous	2,255
essv10779493	deletion	SAMN00009103	Sequencing	Read depth and paired-end mapping	Homozygous	2,711
essv10779494	deletion	SAMN00006381	Sequencing	Read depth and paired-end mapping	Heterozygous	2,721
essv10779495	deletion	SAMN00006386	Sequencing	Read depth and paired-end mapping	Heterozygous	2,544
essv10779496	deletion	SAMN00006387	Sequencing	Read depth and paired-end mapping	Heterozygous	2,527
essv10779497	deletion	SAMN00006388	Sequencing	Read depth and paired-end mapping	Heterozygous	2,552
essv10779498	deletion	SAMN00006389	Sequencing	Read depth and paired-end mapping	Heterozygous	2,489
essv10779499	deletion	SAMN00009105	Sequencing	Read depth and paired-end mapping	Heterozygous	2,596
essv10779500	deletion	SAMN00009106	Sequencing	Read depth and paired-end mapping	Heterozygous	2,582
essv10779501	deletion	SAMN00006393	Sequencing	Read depth and paired-end mapping	Heterozygous	2,531
essv10779502	deletion	SAMN00006395	Sequencing	Read depth and paired-end mapping	Heterozygous	2,553
essv10779503	deletion	SAMN00009112	Sequencing	Read depth and paired-end mapping	Heterozygous	2,788
essv10779504	deletion	SAMN00006397	Sequencing	Read depth and paired-end mapping	Homozygous	2,768
essv10779505	deletion	SAMN00006399	Sequencing	Read depth and paired-end mapping	Heterozygous	2,300
essv10779506	deletion	SAMN00006400	Sequencing	Read depth and paired-end mapping	Heterozygous	2,782
essv10779507	deletion	SAMN00006404	Sequencing	Read depth and paired-end mapping	Heterozygous	2,621
essv10779508	deletion	SAMN00006413	Sequencing	Read depth and paired-end mapping	Homozygous	2,645
essv10779509	deletion	SAMN00006414	Sequencing	Read depth and paired-end mapping	Heterozygous	2,676
essv10779510	deletion	SAMN00006415	Sequencing	Read depth and paired-end mapping	Homozygous	2,782
essv10779511	deletion	SAMN00006417	Sequencing	Read depth and paired-end mapping	Heterozygous	2,428
essv10779512	deletion	SAMN00006419	Sequencing	Read depth and paired-end mapping	Heterozygous	2,762
essv10779513	deletion	SAMN00006420	Sequencing	Read depth and paired-end mapping	Heterozygous	2,805
essv10779514	deletion	SAMN00006422	Sequencing	Read depth and paired-end mapping	Heterozygous	2,348
essv10779515	deletion	SAMN00006424	Sequencing	Read depth and paired-end mapping	Heterozygous	2,745
essv10779516	deletion	SAMN00006428	Sequencing	Read depth and paired-end mapping	Heterozygous	2,754
essv10779517	deletion	SAMN00009113	Sequencing	Read depth and paired-end mapping	Heterozygous	2,679
essv10779518	deletion	SAMN00006433	Sequencing	Read depth and paired-end mapping	Heterozygous	2,389
essv10779519	deletion	SAMN00006435	Sequencing	Read depth and paired-end mapping	Heterozygous	2,697
essv10779520	deletion	SAMN00006436	Sequencing	Read depth and paired-end mapping	Heterozygous	2,677
essv10779521	deletion	SAMN00006441	Sequencing	Read depth and paired-end mapping	Heterozygous	2,819
essv10779522	deletion	SAMN00006447	Sequencing	Read depth and paired-end mapping	Heterozygous	2,620
essv10779523	deletion	SAMN00004686	Sequencing	Read depth and paired-end mapping	Heterozygous	2,749
essv10779524	deletion	SAMN00004696	Sequencing	Read depth and paired-end mapping	Heterozygous	2,738
essv10779525	deletion	SAMN00006472	Sequencing	Read depth and paired-end mapping	Heterozygous	2,390
essv10779526	deletion	SAMN00006480	Sequencing	Read depth and paired-end mapping	Heterozygous	2,619
essv10779527	deletion	SAMN00009114	Sequencing	Read depth and paired-end mapping	Heterozygous	2,651
essv10779528	deletion	SAMN00006499	Sequencing	Read depth and paired-end mapping	Heterozygous	2,590
essv10779529	deletion	SAMN00006501	Sequencing	Read depth and paired-end mapping	Heterozygous	2,700
essv10779530	deletion	SAMN00006508	Sequencing	Read depth and paired-end mapping	Heterozygous	2,890
essv10779531	deletion	SAMN00006520	Sequencing	Read depth and paired-end mapping	Heterozygous	2,560
essv10779532	deletion	SAMN00006522	Sequencing	Read depth and paired-end mapping	Heterozygous	2,639
essv10779533	deletion	SAMN01036848	Sequencing	Read depth and paired-end mapping	Heterozygous	2,751
essv10779534	deletion	SAMN01036849	Sequencing	Read depth and paired-end mapping	Heterozygous	2,759
essv10779535	deletion	SAMN00006535	Sequencing	Read depth and paired-end mapping	Heterozygous	2,682
essv10779536	deletion	SAMN00006537	Sequencing	Read depth and paired-end mapping	Heterozygous	2,790
essv10779537	deletion	SAMN00006544	Sequencing	Read depth and paired-end mapping	Heterozygous	2,575
essv10779538	deletion	SAMN00006546	Sequencing	Read depth and paired-end mapping	Heterozygous	2,722

Showing 100 of 1244

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv10779439	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779440	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779441	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779442	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779443	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779444	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779445	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779446	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779447	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779448	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779449	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779450	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779451	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779452	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779453	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779454	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779455	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779456	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779457	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779458	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779459	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779460	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779461	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779462	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779463	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779464	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779465	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779466	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779467	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779468	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779469	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779470	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779471	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779472	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779473	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779474	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779475	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779476	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779477	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779478	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779479	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779480	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779481	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779482	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779483	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779484	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779485	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779486	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779487	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779488	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779489	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779490	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779491	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779492	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779493	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779494	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779495	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779496	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779497	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779498	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779499	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779500	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779501	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779502	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779503	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779504	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779505	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779506	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779507	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779508	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779509	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779510	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779511	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779512	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779513	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779514	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779515	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779516	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779517	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779518	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779519	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779520	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779521	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779522	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779523	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779524	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779525	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779526	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779527	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779528	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779529	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779530	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779531	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779532	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779533	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779534	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779535	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779536	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779537	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)
essv10779538	Remapped	Perfect	NC_000002.12:g.(17 9199556_179201056) _(179216792_179218 292)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	179,200,556 (-1000, +500)	179,217,292 (-500, +1000)

Showing 100 of 2488

dbVar

Database of genomic structural variation

esv3593502

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Variant Region Placement Information

Variant Call Information

Variant Call Placement Information

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.