A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv959882



Internal ID16253838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:20389440..20461637hg38UCSC Ensembl
Innerchr3:20430932..20503129hg19UCSC Ensembl
Innerchr3:20405936..20478133hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3872198
hg1972198
hg1872198
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589862
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv959882
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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