A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587511



Internal ID16028234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41474022..41475289hg38UCSC Ensembl
Innerchr21:42845949..42847216hg19UCSC Ensembl
Innerchr21:41767819..41769086hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381268
hg191268
hg181268
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7838n54
Supporting Variantsnssv946826
Samples
Known GenesTMPRSS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587511
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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