A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587539



Internal ID16028262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41480393..41504520hg38UCSC Ensembl
Innerchr21:42852320..42876447hg19UCSC Ensembl
Innerchr21:41774190..41798317hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3824128
hg1924128
hg1824128
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv947038
Samples
Known GenesTMPRSS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587539
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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