esv3625715

Organism: Homo sapiens

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

Variant Calls:51
Validation:Not tested
Clinical Assertions: No
Region Size:22,660

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: 352 SVs from 70 studies. See in: genome view

Remapped(Score: Perfect):25,583,969-25,608,628

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3625715	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
esv3625715	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv14065415	deletion	SAMN00006820	Sequencing	Read depth and paired-end mapping	Heterozygous	2,877
essv14065416	deletion	SAMN00262972	Sequencing	Read depth and paired-end mapping	Heterozygous	3,149
essv14065417	deletion	SAMN00262987	Sequencing	Read depth and paired-end mapping	Heterozygous	3,325
essv14065418	deletion	SAMN00630219	Sequencing	Read depth and paired-end mapping	Heterozygous	3,239
essv14065419	deletion	SAMN00630215	Sequencing	Read depth and paired-end mapping	Heterozygous	3,137
essv14065420	deletion	SAMN00630232	Sequencing	Read depth and paired-end mapping	Heterozygous	3,247
essv14065421	deletion	SAMN01091054	Sequencing	Read depth and paired-end mapping	Heterozygous	3,333
essv14065422	deletion	SAMN00779948	Sequencing	Read depth and paired-end mapping	Heterozygous	3,126
essv14065423	deletion	SAMN00779960	Sequencing	Read depth and paired-end mapping	Heterozygous	3,258
essv14065424	deletion	SAMN00779979	Sequencing	Read depth and paired-end mapping	Heterozygous	3,212
essv14065425	deletion	SAMN01036721	Sequencing	Read depth and paired-end mapping	Heterozygous	3,162
essv14065426	deletion	SAMN01036722	Sequencing	Read depth and paired-end mapping	Heterozygous	3,116
essv14065427	deletion	SAMN01036733	Sequencing	Read depth and paired-end mapping	Heterozygous	3,100
essv14065428	deletion	SAMN01761226	Sequencing	Read depth and paired-end mapping	Heterozygous	3,196
essv14065429	deletion	SAMN01090748	Sequencing	Read depth and paired-end mapping	Homozygous	2,921
essv14065430	deletion	SAMN01036746	Sequencing	Read depth and paired-end mapping	Heterozygous	3,278
essv14065431	deletion	SAMN01036752	Sequencing	Read depth and paired-end mapping	Heterozygous	3,109
essv14065432	deletion	SAMN01090796	Sequencing	Read depth and paired-end mapping	Heterozygous	3,016
essv14065433	deletion	SAMN01036783	Sequencing	Read depth and paired-end mapping	Heterozygous	3,166
essv14065434	deletion	SAMN01036784	Sequencing	Read depth and paired-end mapping	Heterozygous	3,195
essv14065435	deletion	SAMN01036810	Sequencing	Read depth and paired-end mapping	Heterozygous	3,221
essv14065436	deletion	SAMN01090876	Sequencing	Read depth and paired-end mapping	Heterozygous	3,009
essv14065437	deletion	SAMN01761295	Sequencing	Read depth and paired-end mapping	Heterozygous	3,217
essv14065438	deletion	SAMN01761302	Sequencing	Read depth and paired-end mapping	Heterozygous	3,284
essv14065439	deletion	SAMN01761319	Sequencing	Read depth and paired-end mapping	Heterozygous	3,229
essv14065440	deletion	SAMN01090900	Sequencing	Read depth and paired-end mapping	Heterozygous	3,077
essv14065441	deletion	SAMN01090791	Sequencing	Read depth and paired-end mapping	Heterozygous	2,952
essv14065442	deletion	SAMN01090769	Sequencing	Read depth and paired-end mapping	Heterozygous	2,975
essv14065443	deletion	SAMN01761345	Sequencing	Read depth and paired-end mapping	Heterozygous	2,565
essv14065444	deletion	SAMN01090822	Sequencing	Read depth and paired-end mapping	Heterozygous	3,090
essv14065445	deletion	SAMN00000415	Sequencing	Read depth and paired-end mapping	Heterozygous	3,187
essv14065446	deletion	SAMN00001580	Sequencing	Read depth and paired-end mapping	Heterozygous	3,286
essv14065447	deletion	SAMN00001581	Sequencing	Read depth and paired-end mapping	Heterozygous	3,289
essv14065448	deletion	SAMN00001590	Sequencing	Read depth and paired-end mapping	Heterozygous	3,076
essv14065449	deletion	SAMN00001059	Sequencing	Read depth and paired-end mapping	Heterozygous	3,175
essv14065450	deletion	SAMN00001673	Sequencing	Read depth and paired-end mapping	Heterozygous	3,256
essv14065451	deletion	SAMN00001687	Sequencing	Read depth and paired-end mapping	Heterozygous	2,530
essv14065452	deletion	SAMN00001100	Sequencing	Read depth and paired-end mapping	Heterozygous	2,868
essv14065453	deletion	SAMN00001110	Sequencing	Read depth and paired-end mapping	Heterozygous	3,124
essv14065454	deletion	SAMN00001112	Sequencing	Read depth and paired-end mapping	Heterozygous	2,972
essv14065455	deletion	SAMN00001125	Sequencing	Read depth and paired-end mapping	Heterozygous	3,001
essv14065456	deletion	SAMN00001146	Sequencing	Read depth and paired-end mapping	Heterozygous	3,120
essv14065457	deletion	SAMN00001150	Sequencing	Read depth and paired-end mapping	Heterozygous	3,142
essv14065458	deletion	SAMN00001160	Sequencing	Read depth and paired-end mapping	Heterozygous	2,641
essv14065459	deletion	SAMN00001164	Sequencing	Read depth and paired-end mapping	Heterozygous	2,395
essv14065460	deletion	SAMN00001167	Sequencing	Read depth and paired-end mapping	Heterozygous	3,363
essv14065461	deletion	SAMN00001181	Sequencing	Read depth and paired-end mapping	Heterozygous	2,491
essv14065462	deletion	SAMN00001186	Sequencing	Read depth and paired-end mapping	Heterozygous	3,005
essv14065463	deletion	SAMN00001192	Sequencing	Read depth and paired-end mapping	Heterozygous	3,071
essv14065464	deletion	SAMN00001193	Sequencing	Read depth and paired-end mapping	Heterozygous	3,046
essv14065465	deletion	SAMN00001275	Sequencing	Read depth and paired-end mapping	Heterozygous	2,790

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv14065415	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065416	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065417	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065418	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065419	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065420	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065421	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065422	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065423	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065424	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065425	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065426	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065427	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065428	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065429	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065430	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065431	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065432	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065433	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065434	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065435	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065436	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065437	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065438	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065439	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065440	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065441	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065442	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065443	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065444	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065445	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065446	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065447	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065448	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065449	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065450	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065451	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065452	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065453	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065454	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065455	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065456	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065457	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065458	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065459	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065460	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065461	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065462	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065463	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065464	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065465	Remapped	Perfect	NC_000011.10:g.(25 583969_25585469)_( 25607128_25608628) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	25,584,969 (-1000, +500)	25,607,628 (-500, +1000)
essv14065415	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065416	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065417	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065418	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065419	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065420	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065421	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065422	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065423	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065424	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065425	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065426	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065427	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065428	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065429	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065430	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065431	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065432	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065433	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065434	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065435	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065436	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065437	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065438	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065439	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065440	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065441	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065442	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065443	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065444	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065445	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065446	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065447	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065448	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065449	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065450	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065451	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065452	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065453	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065454	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065455	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065456	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065457	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065458	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065459	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065460	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065461	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065462	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)
essv14065463	Submitted genomic		NC_000011.9:g.(256 05515_25607015)_(2 5628674_25630174)d el	GRCh37 (hg19)		NC_000011.9	Chr11	25,606,515 (-1000, +500)	25,629,174 (-500, +1000)

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dbVar

Database of genomic structural variation

esv3625715

Links to Other Resources

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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.