A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891425



Internal ID19185821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:83046693..83244356hg38UCSC Ensembl
Outerchr8:83046693..83244356hg38UCSC Ensembl
Innerchr8:83958928..84156591hg19UCSC Ensembl
Outerchr8:83958928..84156591hg19UCSC Ensembl
Innerchr8:84121483..84319146hg18UCSC Ensembl
Outerchr8:84121483..84319146hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38197664
hg19197664
hg18197664
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787964
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891425
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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