A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7835n54



Internal ID19000011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41469683..41475581hg38UCSC Ensembl
chr21:42841610..42847508hg19UCSC Ensembl
chr21:41763480..41769378hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg385899
hg195899
hg185899
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587499, nsv587498
Samples
Known GenesTMPRSS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7835n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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