esv3626720

Organism: Homo sapiens

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

Variant Calls:39
Validation:Not tested
Clinical Assertions: No
Region Size:229,378

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: 916 SVs from 92 studies. See in: genome view

Remapped(Score: Perfect):67,737,871-67,969,248

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3626720	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
esv3626720	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv14198459	deletion	SAMN01036840	Sequencing	Read depth and paired-end mapping	Heterozygous	2,779
essv14198460	deletion	SAMN00006439	Sequencing	Read depth and paired-end mapping	Heterozygous	2,803
essv14198461	deletion	SAMN00006462	Sequencing	Read depth and paired-end mapping	Heterozygous	2,676
essv14198462	deletion	SAMN00006472	Sequencing	Read depth and paired-end mapping	Heterozygous	2,390
essv14198463	deletion	SAMN00006541	Sequencing	Read depth and paired-end mapping	Heterozygous	2,595
essv14198464	deletion	SAMN00006544	Sequencing	Read depth and paired-end mapping	Heterozygous	2,575
essv14198465	deletion	SAMN00006564	Sequencing	Read depth and paired-end mapping	Heterozygous	2,673
essv14198466	deletion	SAMN00006573	Sequencing	Read depth and paired-end mapping	Heterozygous	2,632
essv14198467	deletion	SAMN00249886	Sequencing	Read depth and paired-end mapping	Heterozygous	2,898
essv14198468	deletion	SAMN00009204	Sequencing	Read depth and paired-end mapping	Heterozygous	2,232
essv14198469	deletion	SAMN01091112	Sequencing	Read depth and paired-end mapping	Heterozygous	2,761
essv14198470	deletion	SAMN00249815	Sequencing	Read depth and paired-end mapping	Heterozygous	2,729
essv14198471	deletion	SAMN00249835	Sequencing	Read depth and paired-end mapping	Heterozygous	2,717
essv14198472	deletion	SAMN00249780	Sequencing	Read depth and paired-end mapping	Heterozygous	2,799
essv14198473	deletion	SAMN00630256	Sequencing	Read depth and paired-end mapping	Heterozygous	2,874
essv14198474	deletion	SAMN00249850	Sequencing	Read depth and paired-end mapping	Heterozygous	2,524
essv14198475	deletion	SAMN00630265	Sequencing	Read depth and paired-end mapping	Heterozygous	2,554
essv14198476	deletion	SAMN00249856	Sequencing	Read depth and paired-end mapping	Heterozygous	2,571
essv14198477	deletion	SAMN01091148	Sequencing	Read depth and paired-end mapping	Heterozygous	2,816
essv14198478	deletion	SAMN01090995	Sequencing	Read depth and paired-end mapping	Heterozygous	2,830
essv14198479	deletion	SAMN01761483	Sequencing	Read depth and paired-end mapping	Heterozygous	2,855
essv14198480	deletion	SAMN01096802	Sequencing	Read depth and paired-end mapping	Heterozygous	2,669
essv14198481	deletion	SAMN00000918	Sequencing	Read depth and paired-end mapping	Heterozygous	2,753
essv14198482	deletion	SAMN00000926	Sequencing	Read depth and paired-end mapping	Heterozygous	2,701
essv14198483	deletion	SAMN00001613	Sequencing	Read depth and paired-end mapping	Heterozygous	2,852
essv14198484	deletion	SAMN00001616	Sequencing	Read depth and paired-end mapping	Heterozygous	2,760
essv14198485	deletion	SAMN00000430	Sequencing	Read depth and paired-end mapping	Heterozygous	2,736
essv14198486	deletion	SAMN00001620	Sequencing	Read depth and paired-end mapping	Heterozygous	2,821
essv14198487	deletion	SAMN00001621	Sequencing	Read depth and paired-end mapping	Heterozygous	2,538
essv14198488	deletion	SAMN00000437	Sequencing	Read depth and paired-end mapping	Heterozygous	2,783
essv14198489	deletion	SAMN00000446	Sequencing	Read depth and paired-end mapping	Heterozygous	2,891
essv14198490	deletion	SAMN00000448	Sequencing	Read depth and paired-end mapping	Heterozygous	2,692
essv14198491	deletion	SAMN00000939	Sequencing	Read depth and paired-end mapping	Heterozygous	2,198
essv14198492	deletion	SAMN00001638	Sequencing	Read depth and paired-end mapping	Heterozygous	2,808
essv14198493	deletion	SAMN00001650	Sequencing	Read depth and paired-end mapping	Heterozygous	2,209
essv14198494	deletion	SAMN00000497	Sequencing	Read depth and paired-end mapping	Heterozygous	2,523
essv14198495	deletion	SAMN00000543	Sequencing	Read depth and paired-end mapping	Homozygous	2,556
essv14198496	deletion	SAMN00001258	Sequencing	Read depth and paired-end mapping	Heterozygous	2,841
essv14198497	deletion	SAMN00001273	Sequencing	Read depth and paired-end mapping	Heterozygous	2,823

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv14198459	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198460	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198461	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198462	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198463	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198464	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198465	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198466	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198467	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198468	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198469	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198470	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198471	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198472	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198473	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198474	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198475	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198476	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198477	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198478	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198479	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198480	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198481	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198482	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198483	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198484	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198485	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198486	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198487	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198488	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198489	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198490	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198491	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198492	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198493	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198494	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198495	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198496	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198497	Remapped	Perfect	NC_000011.10:g.(67 737871_67739371)_( 67967748_67969248) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,738,871 (-1000, +500)	67,968,248 (-500, +1000)
essv14198459	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198460	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198461	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198462	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198463	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198464	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198465	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198466	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198467	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198468	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198469	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198470	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198471	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198472	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198473	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198474	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198475	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198476	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198477	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198478	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198479	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198480	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198481	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198482	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198483	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198484	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198485	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198486	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198487	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198488	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198489	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198490	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198491	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198492	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198493	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198494	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198495	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198496	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)
essv14198497	Submitted genomic		NC_000011.9:g.(675 05342_67506842)_(6 7735219_67736719)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,506,342 (-1000, +500)	67,735,719 (-500, +1000)

dbVar

Database of genomic structural variation

esv3626720

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.