A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614377



Internal ID7001271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103452486..103456121hg38UCSC Ensembl
Innerchr7:103452486..103456121hg38UCSC Ensembl
Outerchr7:103452040..103456567hg38UCSC Ensembl
chr7:103092933..103096568hg19UCSC Ensembl
Innerchr7:103092933..103096568hg19UCSC Ensembl
Outerchr7:103092487..103097014hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg383636
hg193636
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12913101, essv12913098, essv12913073, essv12913077, essv12913106, essv12913108, essv12913115, essv12913116, essv12913093, essv12913099, essv12913066, essv12913112, essv12913079, essv12913072, essv12913086, essv12913068, essv12913097, essv12913107, essv12913064, essv12913065, essv12913104, essv12913083, essv12913062, essv12913120, essv12913095, essv12913089, essv12913069, essv12913071, essv12913111, essv12913103, essv12913096, essv12913094, essv12913063, essv12913121, essv12913100, essv12913110, essv12913114, essv12913113, essv12913082, essv12913075, essv12913092, essv12913081, essv12913090, essv12913088, essv12913076, essv12913109, essv12913091, essv12913122, essv12913118, essv12913074, essv12913061, essv12913119, essv12913067, essv12913123, essv12913087, essv12913102, essv12913084, essv12913070, essv12913117, essv12913078, essv12913060, essv12913085, essv12913080, essv12913105
SamplesHG01986, HG02574, NA19700, HG02496, HG02973, HG03175, NA18507, HG03449, HG02798, NA20321, HG03297, NA19443, NA19098, NA18510, HG03086, HG02281, HG03520, HG02315, NA18874, NA19137, HG02461, NA19172, NA18520, HG02879, HG02820, NA19707, HG03061, HG02345, NA19152, NA19236, HG02554, NA19982, HG02817, NA18856, HG02309, NA20282, HG03451, HG02979, NA19160, NA19395, NA18858, HG02568, HG03064, HG02813, HG01444, NA19147, HG02546, HG01958, HG02837, NA19835, HG03557, HG02971, HG03157, HG02970, HG03025, HG02646, NA19185, HG02051, HG01883, NA18505, NA19316, HG02851, HG03118, HG03439
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614377
Frequency
Sample Size2504
Observed Gain0
Observed Loss64
Observed Complex0
Frequencyn/a


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