A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788030



Internal ID19164693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:80605732..80988755hg38UCSC Ensembl
Innerchr3:80654883..81037906hg19UCSC Ensembl
Innerchr3:80737573..81120596hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38383024
hg19383024
hg18383024
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893728
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=43
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788030
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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