A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622814



Internal ID7009672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31752153..31759303hg38UCSC Ensembl
Innerchr10:31752231..31759226hg38UCSC Ensembl
Outerchr10:31752076..31759381hg38UCSC Ensembl
chr10:32041081..32048231hg19UCSC Ensembl
Innerchr10:32041159..32048154hg19UCSC Ensembl
Outerchr10:32041004..32048309hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg387151
hg197151
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13749629, essv13749632, essv13749628, essv13749631, essv13749633, essv13749630
SamplesHG01070, NA20340, HG01396, NA19468, NA19146, HG01061
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622814
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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