A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7587n54



Internal ID22775482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45575651..45577280hg38UCSC Ensembl
chr20:44204290..44205919hg19UCSC Ensembl
chr20:43637704..43639333hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg381630
hg191630
hg181630
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586084, nsv586082, nsv586083
Samples
Known GenesWFDC8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7587n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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