A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv957796



Internal ID15905066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:192626..321571hg38UCSC Ensembl
Innerchr3:234309..363254hg19UCSC Ensembl
Innerchr3:209309..338254hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38128946
hg19128946
hg18128946
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589283
Supporting Variants
Samples
Known GenesCHL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv957796
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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