esv3856613

Organism: Homo sapiens

Study:estd219 (1000 Genomes Consortium Phase 3 Integrated SV)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:36
Validation:Not tested
Clinical Assertions: No
Region Size:37,960

Publication(s):1000 Genomes Consortium Phase 3 Integrated SV

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: 1582 SVs from 76 studies. See in: genome view

Remapped(Score: Perfect):12,073,419-12,112,378

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3856613	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
esv3856613	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv21479539	deletion	HG00155	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,605
essv21479540	deletion	HG00599	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,451
essv21479541	deletion	HG00610	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,303
essv21479542	deletion	HG00629	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,943
essv21479543	deletion	HG00651	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,202
essv21479544	deletion	HG00743	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,757
essv21479545	deletion	HG01070	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,370
essv21479546	deletion	HG01073	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,366
essv21479547	deletion	HG01113	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,811
essv21479548	deletion	HG01384	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,088
essv21479549	deletion	HG01491	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,598
essv21479550	deletion	HG01598	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,387
essv21479551	deletion	HG01812	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,403
essv21479552	deletion	HG01813	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,439
essv21479553	deletion	HG02128	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,574
essv21479554	deletion	HG02700	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,426
essv21479555	deletion	HG03388	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,983
essv21479556	deletion	HG03567	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,389
essv21479557	deletion	HG03694	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,573
essv21479558	deletion	HG04134	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,083
essv21479559	deletion	HG04161	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,729
essv21479560	deletion	HG04206	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,791
essv21479561	deletion	NA18544	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,559
essv21479562	deletion	NA18618	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,911
essv21479563	deletion	NA18626	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,468
essv21479564	deletion	NA18647	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,460
essv21479565	deletion	NA18946	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,177
essv21479566	deletion	NA18959	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,528
essv21479567	deletion	NA18983	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,716
essv21479568	deletion	NA19006	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,645
essv21479569	deletion	NA19067	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,784
essv21479570	deletion	NA19222	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,939
essv21479571	deletion	NA19403	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,594
essv21479572	deletion	NA20863	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,682
essv21479573	deletion	NA21107	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,587
essv21479574	deletion	NA21141	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,407

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv21479539	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479540	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479541	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479542	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479543	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479544	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479545	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479546	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479547	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479548	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479549	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479550	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479551	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479552	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479553	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479554	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479555	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479556	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479557	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479558	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479559	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479560	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479561	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479562	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479563	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479564	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479565	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479566	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479567	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479568	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479569	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479570	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479571	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479572	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479573	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479574	Remapped	Perfect	NC_000009.12:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh38.p12	First Pass	NC_000009.12	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479539	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479540	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479541	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479542	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479543	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479544	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479545	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479546	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479547	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479548	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479549	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479550	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479551	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479552	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479553	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479554	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479555	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479556	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479557	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479558	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479559	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479560	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479561	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479562	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479563	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479564	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479565	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479566	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479567	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479568	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479569	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479570	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479571	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479572	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479573	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)
essv21479574	Submitted genomic		NC_000009.11:g.(12 073419_12073919)_( 12111878_12112378) del	GRCh37 (hg19)		NC_000009.11	Chr9	12,073,919 (-500, +0)	12,111,878 (-0, +500)

dbVar

Database of genomic structural variation

esv3856613

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.