A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7840n54



Internal ID19000016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41474124..41475776hg38UCSC Ensembl
chr21:42846051..42847703hg19UCSC Ensembl
chr21:41767921..41769573hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381653
hg191653
hg181653
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587525, nsv587518, nsv587527, nsv587521, nsv587522, nsv587531, nsv587526
Samples
Known GenesTMPRSS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7840n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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