A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587509



Internal ID16028232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41474022..41474980hg38UCSC Ensembl
Innerchr21:42845949..42846907hg19UCSC Ensembl
Innerchr21:41767819..41768777hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38959
hg19959
hg18959
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946821, nssv946822, nssv946823
Samples
Known GenesTMPRSS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587509
Frequency
Sample Size17421
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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