A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569832



Internal ID16357241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71183826..71185161hg38UCSC Ensembl
Innerchr15:71476165..71477500hg19UCSC Ensembl
Innerchr15:69263219..69264554hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381336
hg191336
hg181336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4589n54
Supporting Variantsnssv844428, nssv844427
Samples
Known GenesTHSD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569832
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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