A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7645n54



Internal ID22775540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62064345..62066675hg38UCSC Ensembl
chr20:60639401..60641731hg19UCSC Ensembl
chr20:60072796..60075126hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg382331
hg192331
hg182331
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586457, nsv586467, nsv586464, nsv586459, nsv586454
Samples
Known GenesTAF4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7645n54
Frequency
Sample Size17421
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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