A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7589n54



Internal ID20141013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45575651..45583998hg38UCSC Ensembl
chr20:44204290..44212637hg19UCSC Ensembl
chr20:43637704..43646051hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg388348
hg198348
hg188348
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586106, nsv586090
Samples
Known GenesWFDC8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7589n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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