A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv963682



Internal ID16257638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65194244..65225832hg38UCSC Ensembl
Innerchr3:65179919..65211507hg19UCSC Ensembl
Innerchr3:65154959..65186547hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3831589
hg1931589
hg1831589
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590479
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)nssv963682
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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