A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787878



Internal ID19172456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:28621186..28746968hg38UCSC Ensembl
Innerchr5:28621293..28747075hg19UCSC Ensembl
Innerchr5:28657050..28782832hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg38125783
hg19125783
hg18125783
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894160
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=24
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787878
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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