A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569838



Internal ID16357247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71184117..71185654hg38UCSC Ensembl
Innerchr15:71476456..71477993hg19UCSC Ensembl
Innerchr15:69263510..69265047hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381538
hg191538
hg181538
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4590n54
Supporting Variantsnssv844446
Samples
Known GenesTHSD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569838
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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