A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7562n54



Internal ID18999738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34654732..34655798hg38UCSC Ensembl
chr20:33242536..33243602hg19UCSC Ensembl
chr20:32706197..32707263hg18UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg381067
hg191067
hg181067
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv585936, nsv585938, nsv585937, nsv585935, nsv585939
Samples
Known GenesPIGU
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7562n54
Frequency
Sample Size17421
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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