A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622828



Internal ID7009686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32351820..32356489hg38UCSC Ensembl
Innerchr10:32351840..32356470hg38UCSC Ensembl
Outerchr10:32351801..32356509hg38UCSC Ensembl
chr10:32640748..32645417hg19UCSC Ensembl
Innerchr10:32640768..32645398hg19UCSC Ensembl
Outerchr10:32640729..32645437hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg384670
hg194670
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13749904
SamplesNA12872
Known GenesEPC1, LOC102031319
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622828
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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