A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7561n54



Internal ID18999737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34654522..34655852hg38UCSC Ensembl
chr20:33242326..33243656hg19UCSC Ensembl
chr20:32705987..32707317hg18UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg381331
hg191331
hg181331
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv585932, nsv585934
Samples
Known GenesPIGU
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7561n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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