A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv982921



Internal ID16276877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:189647176..189649762hg38UCSC Ensembl
Innerchr3:189364965..189367551hg19UCSC Ensembl
Innerchr3:190847659..190850245hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg382587
hg192587
hg182587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592766
Supporting Variants
Samples
Known GenesTP63
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv982921
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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