A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv979632



Internal ID15926902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163001200..163004174hg38UCSC Ensembl
Innerchr3:162718988..162721962hg19UCSC Ensembl
Innerchr3:164201682..164204656hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg382975
hg192975
hg182975
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592364
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)nssv979632
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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