A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv946828



Internal ID15894098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41474022..41475394hg38UCSC Ensembl
Innerchr21:42845949..42847321hg19UCSC Ensembl
Innerchr21:41767819..41769191hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381373
hg191373
hg181373
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587512
Supporting Variants
Samples
Known GenesTMPRSS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv946828
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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