A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592767



Internal ID16380176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:189647176..189650119hg38UCSC Ensembl
Innerchr3:189364965..189367908hg19UCSC Ensembl
Innerchr3:190847659..190850602hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg382944
hg192944
hg182944
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8779n54
Supporting Variantsnssv982923, nssv982924
Samples
Known GenesTP63
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592767
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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