A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv920073



Internal ID15867343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:132409690..132603709hg38UCSC Ensembl
Innerchr2:133167263..133361282hg19UCSC Ensembl
Innerchr2:132883733..133077752hg18UCSC Ensembl
Cytoband2q21.2
Allele length
AssemblyAllele length
hg38194020
hg19194020
hg18194020
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv583153
Supporting Variants
Samples
Known GenesGPR39
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv920073
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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