A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv947027



Internal ID15894297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41474668..41475581hg38UCSC Ensembl
Innerchr21:42846595..42847508hg19UCSC Ensembl
Innerchr21:41768465..41769378hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38914
hg19914
hg18914
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587535
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)nssv947027
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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