A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv946824



Internal ID15894094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41474022..41475068hg38UCSC Ensembl
Innerchr21:42845949..42846995hg19UCSC Ensembl
Innerchr21:41767819..41768865hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381047
hg191047
hg181047
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587510
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)nssv946824
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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