A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7841n54



Internal ID19000017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41474344..41475509hg38UCSC Ensembl
chr21:42846271..42847436hg19UCSC Ensembl
chr21:41768141..41769306hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381166
hg191166
hg181166
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587530, nsv587533, nsv587534, nsv587529, nsv587532
Samples
Known GenesTMPRSS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7841n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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