A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv843667



Internal ID16137623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:61910283..62027108hg38UCSC Ensembl
Innerchr15:62202482..62319307hg19UCSC Ensembl
Innerchr15:59989774..60106599hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38116826
hg19116826
hg18116826
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569645
Supporting Variants
Samples
Known GenesVPS13C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv843667
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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