A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788322



Internal ID19177822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89862726..90393775hg38UCSC Ensembl
Innerchr3:89911876..90442925hg19UCSC Ensembl
Innerchr3:89994566..90525615hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38531050
hg19531050
hg18531050
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893741
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=32
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788322
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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