A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv962594



Internal ID15909864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46769856..46799313hg38UCSC Ensembl
Innerchr3:46811346..46840803hg19UCSC Ensembl
Innerchr3:46786350..46815807hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3829458
hg1929458
hg1829458
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590201
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)nssv962594
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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