A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7837n54



Internal ID19000013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41471061..41475776hg38UCSC Ensembl
chr21:42842988..42847703hg19UCSC Ensembl
chr21:41764858..41769573hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg384716
hg194716
hg184716
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587505, nsv587508, nsv587507, nsv587504
Samples
Known GenesTMPRSS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7837n54
Frequency
Sample Size17421
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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