A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788312



Internal ID19161122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:46841409..46878190hg38UCSC Ensembl
Innerchr20:45470048..45506829hg19UCSC Ensembl
Innerchr20:44903455..44940236hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3836782
hg1936782
hg1836782
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893341
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=16
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788312
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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