A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587517



Internal ID16028240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41474022..41479527hg38UCSC Ensembl
Innerchr21:42845949..42851454hg19UCSC Ensembl
Innerchr21:41767819..41773324hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg385506
hg195506
hg185506
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946969
Samples
Known GenesTMPRSS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587517
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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