A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569819



Internal ID16010542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71143283..71409321hg38UCSC Ensembl
Innerchr15:71435622..71701660hg19UCSC Ensembl
Innerchr15:69222676..69488714hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38266039
hg19266039
hg18266039
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149241
SamplesHGDP01030
Known GenesTHSD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569819
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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