esv3612805

Organism: Homo sapiens

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

Variant Calls:54
Validation:Not tested
Clinical Assertions: No
Region Size:18,108

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: 178 SVs from 49 studies. See in: genome view

Remapped(Score: Perfect):34,856,063-34,874,195

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3612805	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
esv3612805	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv12726542	deletion	SAMN01091083	Sequencing	Read depth and paired-end mapping	Heterozygous	2,265
essv12726543	deletion	SAMN01091133	Sequencing	Read depth and paired-end mapping	Heterozygous	2,963
essv12726544	deletion	SAMN00262968	Sequencing	Read depth and paired-end mapping	Heterozygous	3,187
essv12726545	deletion	SAMN00262980	Sequencing	Read depth and paired-end mapping	Heterozygous	2,988
essv12726546	deletion	SAMN00630230	Sequencing	Read depth and paired-end mapping	Heterozygous	3,194
essv12726547	deletion	SAMN00630232	Sequencing	Read depth and paired-end mapping	Heterozygous	3,247
essv12726548	deletion	SAMN01091043	Sequencing	Read depth and paired-end mapping	Heterozygous	2,937
essv12726549	deletion	SAMN01091044	Sequencing	Read depth and paired-end mapping	Heterozygous	2,852
essv12726550	deletion	SAMN01091045	Sequencing	Read depth and paired-end mapping	Heterozygous	3,089
essv12726551	deletion	SAMN00630253	Sequencing	Read depth and paired-end mapping	Heterozygous	3,391
essv12726552	deletion	SAMN01091054	Sequencing	Read depth and paired-end mapping	Heterozygous	3,333
essv12726553	deletion	SAMN01091056	Sequencing	Read depth and paired-end mapping	Heterozygous	3,207
essv12726554	deletion	SAMN01091058	Sequencing	Read depth and paired-end mapping	Heterozygous	2,803
essv12726555	deletion	SAMN00779943	Sequencing	Read depth and paired-end mapping	Heterozygous	3,267
essv12726556	deletion	SAMN00779952	Sequencing	Read depth and paired-end mapping	Heterozygous	3,140
essv12726557	deletion	SAMN01090760	Sequencing	Read depth and paired-end mapping	Heterozygous	3,134
essv12726558	deletion	SAMN01036773	Sequencing	Read depth and paired-end mapping	Heterozygous	2,954
essv12726559	deletion	SAMN01036798	Sequencing	Read depth and paired-end mapping	Heterozygous	3,277
essv12726560	deletion	SAMN01036800	Sequencing	Read depth and paired-end mapping	Heterozygous	3,246
essv12726561	deletion	SAMN01036779	Sequencing	Read depth and paired-end mapping	Heterozygous	3,152
essv12726562	deletion	SAMN01761237	Sequencing	Read depth and paired-end mapping	Heterozygous	3,277
essv12726563	deletion	SAMN01761243	Sequencing	Read depth and paired-end mapping	Heterozygous	3,270
essv12726564	deletion	SAMN01090773	Sequencing	Read depth and paired-end mapping	Heterozygous	2,777
essv12726565	deletion	SAMN01090873	Sequencing	Read depth and paired-end mapping	Heterozygous	3,010
essv12726566	deletion	SAMN01036812	Sequencing	Read depth and paired-end mapping	Heterozygous	3,220
essv12726567	deletion	SAMN01090888	Sequencing	Read depth and paired-end mapping	Heterozygous	3,125
essv12726568	deletion	SAMN01090850	Sequencing	Read depth and paired-end mapping	Heterozygous	2,923
essv12726569	deletion	SAMN01090859	Sequencing	Read depth and paired-end mapping	Heterozygous	2,807
essv12726570	deletion	SAMN01036788	Sequencing	Read depth and paired-end mapping	Heterozygous	3,166
essv12726571	deletion	SAMN01090791	Sequencing	Read depth and paired-end mapping	Heterozygous	2,952
essv12726572	deletion	SAMN01761348	Sequencing	Read depth and paired-end mapping	Heterozygous	3,263
essv12726573	deletion	SAMN01090837	Sequencing	Read depth and paired-end mapping	Heterozygous	3,072
essv12726574	deletion	SAMN01090825	Sequencing	Read depth and paired-end mapping	Heterozygous	3,024
essv12726575	deletion	SAMN01761266	Sequencing	Read depth and paired-end mapping	Heterozygous	2,677
essv12726576	deletion	SAMN00001578	Sequencing	Read depth and paired-end mapping	Heterozygous	3,111
essv12726577	deletion	SAMN00001585	Sequencing	Read depth and paired-end mapping	Heterozygous	3,075
essv12726578	deletion	SAMN00001020	Sequencing	Read depth and paired-end mapping	Heterozygous	3,239
essv12726579	deletion	SAMN00000479	Sequencing	Read depth and paired-end mapping	Heterozygous	3,240
essv12726580	deletion	SAMN00000481	Sequencing	Read depth and paired-end mapping	Heterozygous	2,468
essv12726581	deletion	SAMN00001665	Sequencing	Read depth and paired-end mapping	Heterozygous	3,380
essv12726582	deletion	SAMN00001667	Sequencing	Read depth and paired-end mapping	Heterozygous	3,266
essv12726583	deletion	SAMN00001682	Sequencing	Read depth and paired-end mapping	Heterozygous	2,680
essv12726584	deletion	SAMN00001683	Sequencing	Read depth and paired-end mapping	Heterozygous	2,908
essv12726585	deletion	SAMN00000564	Sequencing	Read depth and paired-end mapping	Heterozygous	2,805
essv12726586	deletion	SAMN00000565	Sequencing	Read depth and paired-end mapping	Heterozygous	3,208
essv12726587	deletion	SAMN00001692	Sequencing	Read depth and paired-end mapping	Heterozygous	3,336
essv12726588	deletion	SAMN00000570	Sequencing	Read depth and paired-end mapping	Heterozygous	2,486
essv12726589	deletion	SAMN00001114	Sequencing	Read depth and paired-end mapping	Heterozygous	2,431
essv12726590	deletion	SAMN00001152	Sequencing	Read depth and paired-end mapping	Heterozygous	3,097
essv12726591	deletion	SAMN00001187	Sequencing	Read depth and paired-end mapping	Heterozygous	2,941
essv12726592	deletion	SAMN00007806	Sequencing	Read depth and paired-end mapping	Heterozygous	3,302
essv12726593	deletion	SAMN00007807	Sequencing	Read depth and paired-end mapping	Heterozygous	3,277
essv12726594	deletion	SAMN00004484	Sequencing	Read depth and paired-end mapping	Heterozygous	2,926
essv12726595	deletion	SAMN00007873	Sequencing	Read depth and paired-end mapping	Heterozygous	2,690

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv12726542	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726543	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726544	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726545	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726546	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726547	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726548	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726549	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726550	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726551	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726552	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726553	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726554	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726555	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726556	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726557	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726558	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726559	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726560	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726561	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726562	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726563	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726564	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726565	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726566	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726567	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726568	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726569	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726570	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726571	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726572	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726573	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726574	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726575	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726576	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726577	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726578	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726579	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726580	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726581	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726582	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726583	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726584	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726585	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726586	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726587	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726588	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726589	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726590	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726591	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726592	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726593	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726594	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726595	Remapped	Perfect	NC_000007.14:g.(34 856063_34856088)_( 34874170_34874195) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	34,856,075 (-12, +13)	34,874,182 (-12, +13)
essv12726542	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726543	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726544	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726545	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726546	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726547	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726548	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726549	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726550	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726551	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726552	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726553	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726554	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726555	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726556	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726557	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726558	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726559	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726560	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726561	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726562	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726563	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726564	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726565	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726566	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726567	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726568	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726569	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726570	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726571	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726572	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726573	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726574	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726575	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726576	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726577	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726578	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726579	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726580	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726581	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726582	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726583	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726584	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726585	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726586	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)
essv12726587	Submitted genomic		NC_000007.13:g.(34 895675_34895700)_( 34913782_34913807) del	GRCh37 (hg19)		NC_000007.13	Chr7	34,895,687 (-12, +13)	34,913,794 (-12, +13)

Showing 100 of 108

dbVar

Database of genomic structural variation

esv3612805

Links to Other Resources

Genome View

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.