A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587503



Internal ID16028226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41471061..41474877hg38UCSC Ensembl
Innerchr21:42842988..42846804hg19UCSC Ensembl
Innerchr21:41764858..41768674hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg383817
hg193817
hg183817
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946799, nssv946800
Samples
Known GenesTMPRSS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587503
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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