A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7874n54



Internal ID19000050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43708309..43771258hg38UCSC Ensembl
chr21:45128190..45191139hg19UCSC Ensembl
chr21:43952618..44015567hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3862950
hg1962950
hg1862950
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587701, nsv587702
Samples
Known GenesPDXK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7874n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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