A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787964



Internal ID19179659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:83046693..83244356hg38UCSC Ensembl
Innerchr8:83958928..84156591hg19UCSC Ensembl
Innerchr8:84121483..84319146hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38197664
hg19197664
hg18197664
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891425
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=36
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787964
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer