A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv962592



Internal ID15909862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46759566..46805202hg38UCSC Ensembl
Innerchr3:46801056..46846692hg19UCSC Ensembl
Innerchr3:46776060..46821696hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3845637
hg1945637
hg1845637
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590200
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)nssv962592
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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