A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv982913



Internal ID16276869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:189646635..189648974hg38UCSC Ensembl
Innerchr3:189364424..189366763hg19UCSC Ensembl
Innerchr3:190847118..190849457hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg382340
hg192340
hg182340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592765
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)nssv982913
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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