A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788153



Internal ID18817823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5233115..5366498hg38UCSC Ensembl
Innerchr10:5275078..5408461hg19UCSC Ensembl
Innerchr10:5265078..5398461hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38133384
hg19133384
hg18133384
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891744
Supporting Variants
Samples
Known GenesUCN3
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=50
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788153
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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