A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149228



Internal ID15528913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:61910283..62227459hg38UCSC Ensembl
Innerchr15:62202482..62519658hg19UCSC Ensembl
Innerchr15:59989774..60306950hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38317177
hg19317177
hg18317177
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569646
Supporting Variants
SamplesHGDP00707
Known GenesC2CD4A, C2CD4B, VPS13C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149228
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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