A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891366



Internal ID19185762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18045537..18054312hg38UCSC Ensembl
Outerchr8:18045537..18054312hg38UCSC Ensembl
Innerchr8:17903046..17911821hg19UCSC Ensembl
Outerchr8:17903046..17911821hg19UCSC Ensembl
Innerchr8:17947326..17956101hg18UCSC Ensembl
Outerchr8:17947326..17956101hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg388776
hg198776
hg188776
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796077
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891366
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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