A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv933654



Internal ID16227610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:237128793..237130869hg38UCSC Ensembl
Innerchr2:238037436..238039512hg19UCSC Ensembl
Innerchr2:237702175..237704251hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg382077
hg192077
hg182077
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584726
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)nssv933654
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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