A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv977488



Internal ID16271444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162413620..162520451hg38UCSC Ensembl
Innerchr3:162131408..162238239hg19UCSC Ensembl
Innerchr3:163614102..163720933hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38106832
hg19106832
hg18106832
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592182
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)nssv977488
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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