A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv946800



Internal ID15894070
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 StatusS
Merged Variantsnsv587503
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)nssv946800
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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