A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv978202



Internal ID16272158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162794895..163051176hg38UCSC Ensembl
Innerchr3:162512683..162768964hg19UCSC Ensembl
Innerchr3:163995377..164251658hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38256282
hg19256282
hg18256282
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592250
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)nssv978202
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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