A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv947039



Internal ID15894309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41498595..41569539hg38UCSC Ensembl
Innerchr21:42870522..42941466hg19UCSC Ensembl
Innerchr21:41792392..41863336hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3870945
hg1970945
hg1870945
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587540
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)nssv947039
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer