A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893341



Internal ID19184161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:46841409..46878190hg38UCSC Ensembl
Outerchr20:46841409..46878190hg38UCSC Ensembl
Innerchr20:45470048..45506829hg19UCSC Ensembl
Outerchr20:45470048..45506829hg19UCSC Ensembl
Innerchr20:44903455..44940236hg18UCSC Ensembl
Outerchr20:44903455..44940236hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3836782
hg1936782
hg1836782
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788312
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893341
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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