A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7686n54



Internal ID22775581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63830660..63836274hg38UCSC Ensembl
chr20:62462013..62467627hg19UCSC Ensembl
chr20:61932457..61938071hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg385615
hg195615
hg185615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586680, nsv586657, nsv586682, nsv586663, nsv586677, nsv586675, nsv586651, nsv586662
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7686n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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