esv3604168

Organism: Homo sapiens

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

Variant Calls:41
Validation:Not tested
Clinical Assertions: No
Region Size:79,101

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: 832 SVs from 84 studies. See in: genome view

Remapped(Score: Perfect):17,526,744-17,605,916

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3604168	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
esv3604168	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv11821525	deletion	SAMN00016970	Sequencing	Read depth and paired-end mapping	Heterozygous	2,824
essv11821526	deletion	SAMN01761624	Sequencing	Read depth and paired-end mapping	Heterozygous	2,255
essv11821527	deletion	SAMN00009106	Sequencing	Read depth and paired-end mapping	Heterozygous	2,582
essv11821528	deletion	SAMN00006393	Sequencing	Read depth and paired-end mapping	Heterozygous	2,531
essv11821529	deletion	SAMN00006409	Sequencing	Read depth and paired-end mapping	Heterozygous	2,477
essv11821530	deletion	SAMN00006580	Sequencing	Read depth and paired-end mapping	Heterozygous	2,978
essv11821531	deletion	SAMN00009186	Sequencing	Read depth and paired-end mapping	Heterozygous	2,841
essv11821532	deletion	SAMN00014372	Sequencing	Read depth and paired-end mapping	Heterozygous	2,821
essv11821533	deletion	SAMN00249875	Sequencing	Read depth and paired-end mapping	Heterozygous	2,992
essv11821534	deletion	SAMN00249826	Sequencing	Read depth and paired-end mapping	Homozygous	2,733
essv11821535	deletion	SAMN00249784	Sequencing	Read depth and paired-end mapping	Heterozygous	2,593
essv11821536	deletion	SAMN00263031	Sequencing	Read depth and paired-end mapping	Heterozygous	2,854
essv11821537	deletion	SAMN00249789	Sequencing	Read depth and paired-end mapping	Heterozygous	2,536
essv11821538	deletion	SAMN00263036	Sequencing	Read depth and paired-end mapping	Heterozygous	2,821
essv11821539	deletion	SAMN00263043	Sequencing	Read depth and paired-end mapping	Heterozygous	2,855
essv11821540	deletion	SAMN00263060	Sequencing	Read depth and paired-end mapping	Heterozygous	2,792
essv11821541	deletion	SAMN01761226	Sequencing	Read depth and paired-end mapping	Heterozygous	3,196
essv11821542	deletion	SAMN01090779	Sequencing	Read depth and paired-end mapping	Heterozygous	2,946
essv11821543	deletion	SAMN01090818	Sequencing	Read depth and paired-end mapping	Heterozygous	3,288
essv11821544	deletion	SAMN01090811	Sequencing	Read depth and paired-end mapping	Heterozygous	3,042
essv11821545	deletion	SAMN01761482	Sequencing	Read depth and paired-end mapping	Heterozygous	2,839
essv11821546	deletion	SAMN00216588	Sequencing	Read depth and paired-end mapping	Heterozygous	2,759
essv11821547	deletion	SAMN00801732	Sequencing	Read depth and paired-end mapping	Heterozygous	2,867
essv11821548	deletion	SAMN00801738	Sequencing	Read depth and paired-end mapping	Heterozygous	2,824
essv11821549	deletion	SAMN00001030	Sequencing	Read depth and paired-end mapping	Heterozygous	2,684
essv11821550	deletion	SAMN00001037	Sequencing	Read depth and paired-end mapping	Heterozygous	2,923
essv11821551	deletion	SAMN00001053	Sequencing	Read depth and paired-end mapping	Heterozygous	2,754
essv11821552	deletion	SAMN00001065	Sequencing	Read depth and paired-end mapping	Heterozygous	2,781
essv11821553	deletion	SAMN00001105	Sequencing	Read depth and paired-end mapping	Heterozygous	2,391
essv11821554	deletion	SAMN00001108	Sequencing	Read depth and paired-end mapping	Heterozygous	2,458
essv11821555	deletion	SAMN00001121	Sequencing	Read depth and paired-end mapping	Heterozygous	3,030
essv11821556	deletion	SAMN00001122	Sequencing	Read depth and paired-end mapping	Heterozygous	3,250
essv11821557	deletion	SAMN00001129	Sequencing	Read depth and paired-end mapping	Heterozygous	3,123
essv11821558	deletion	SAMN00001163	Sequencing	Read depth and paired-end mapping	Heterozygous	2,750
essv11821559	deletion	SAMN00001164	Sequencing	Read depth and paired-end mapping	Heterozygous	2,395
essv11821560	deletion	SAMN00001170	Sequencing	Read depth and paired-end mapping	Heterozygous	3,238
essv11821561	deletion	SAMN00001179	Sequencing	Read depth and paired-end mapping	Heterozygous	3,049
essv11821562	deletion	SAMN00001187	Sequencing	Read depth and paired-end mapping	Heterozygous	2,941
essv11821563	deletion	SAMN00001192	Sequencing	Read depth and paired-end mapping	Heterozygous	3,071
essv11821564	deletion	SAMN00007725	Sequencing	Read depth and paired-end mapping	Heterozygous	2,947
essv11821565	deletion	SAMN00007874	Sequencing	Read depth and paired-end mapping	Heterozygous	3,150

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv11821525	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821526	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821527	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821528	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821529	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821530	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821531	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821532	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821533	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821534	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821535	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821536	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821537	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821538	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821539	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821540	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821541	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821542	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821543	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821544	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821545	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821546	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821547	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821548	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821549	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821550	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821551	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821552	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821553	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821554	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821555	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821556	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821557	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821558	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821559	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821560	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821561	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821562	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821563	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821564	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821565	Remapped	Perfect	NC_000005.10:g.(17 526744_17526816)_( 17605844_17605916) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	17,526,780 (-36, +36)	17,605,880 (-36, +36)
essv11821525	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821526	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821527	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821528	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821529	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821530	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821531	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821532	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821533	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821534	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821535	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821536	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821537	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821538	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821539	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821540	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821541	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821542	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821543	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821544	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821545	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821546	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821547	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821548	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821549	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821550	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821551	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821552	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821553	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821554	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821555	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821556	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821557	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821558	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821559	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821560	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821561	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821562	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821563	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821564	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)
essv11821565	Submitted genomic		NC_000005.9:g.(175 26853_17526925)_(1 7605953_17606025)d el	GRCh37 (hg19)		NC_000005.9	Chr5	17,526,889 (-36, +36)	17,605,989 (-36, +36)

dbVar

Database of genomic structural variation

esv3604168

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.