A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569650



Internal ID16357059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:61950998..62021174hg38UCSC Ensembl
Innerchr15:62243197..62313373hg19UCSC Ensembl
Innerchr15:60030489..60100665hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3870177
hg1970177
hg1870177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4564n54
Supporting Variantsnssv843674, nssv843673
Samples
Known GenesVPS13C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569650
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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