A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624077



Internal ID6664244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:85620398..85622326hg38UCSC Ensembl
Innerchr10:85620399..85622325hg38UCSC Ensembl
Outerchr10:85620397..85622327hg38UCSC Ensembl
chr10:87380155..87382083hg19UCSC Ensembl
Innerchr10:87380156..87382082hg19UCSC Ensembl
Outerchr10:87380154..87382084hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg381929
hg191929
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13882812, essv13882807, essv13882820, essv13882816, essv13882822, essv13882810, essv13882818, essv13882813, essv13882809, essv13882808, essv13882815, essv13882817, essv13882814, essv13882806, essv13882811, essv13882819, essv13882821
SamplesNA21089, HG03926, NA20905, HG03604, HG03832, NA20858, HG04019, HG01102, HG03858, HG01286, HG00126, HG03790, NA20289, HG03998, NA19661, NA20585, NA12154
Known GenesGRID1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624077
Frequency
Sample Size2504
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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