A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569644



Internal ID16357053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:61910283..61954868hg38UCSC Ensembl
Innerchr15:62202482..62247067hg19UCSC Ensembl
Innerchr15:59989774..60034359hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3844586
hg1944586
hg1844586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv843666
Samples
Known GenesVPS13C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569644
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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