A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592773



Internal ID16033496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:189647176..189653225hg38UCSC Ensembl
Innerchr3:189364965..189371014hg19UCSC Ensembl
Innerchr3:190847659..190853708hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg386050
hg196050
hg186050
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv982992, nssv982991
Samples
Known GenesTP63
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592773
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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