A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7518n54



Internal ID22775413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21926142..21987312hg38UCSC Ensembl
chr20:21906780..21967950hg19UCSC Ensembl
chr20:21854780..21915950hg18UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg3861171
hg1961171
hg1861171
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv585716, nsv585718, nsv585715
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7518n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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