A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569649



Internal ID16357058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:61950998..62008895hg38UCSC Ensembl
Innerchr15:62243197..62301094hg19UCSC Ensembl
Innerchr15:60030489..60088386hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3857898
hg1957898
hg1857898
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4564n54
Supporting Variantsnssv843670, nssv843671, nssv843672
Samples
Known GenesVPS13C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569649
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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