A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622579



Internal ID7009437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21396181..21398145hg38UCSC Ensembl
Innerchr10:21396181..21398145hg38UCSC Ensembl
Outerchr10:21395919..21398435hg38UCSC Ensembl
chr10:21685110..21687074hg19UCSC Ensembl
Innerchr10:21685110..21687074hg19UCSC Ensembl
Outerchr10:21684848..21687364hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg381965
hg191965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13715217, essv13715215, essv13715212, essv13715216, essv13715214, essv13715211, essv13715218, essv13715213
SamplesHG01501, NA20832, HG02789, NA20778, HG03019, HG00342, HG00310, NA20772
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622579
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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