A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894160



Internal ID19185229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:28621186..28746968hg38UCSC Ensembl
Outerchr5:28621186..28746968hg38UCSC Ensembl
Innerchr5:28621293..28747075hg19UCSC Ensembl
Outerchr5:28621293..28747075hg19UCSC Ensembl
Innerchr5:28657050..28782832hg18UCSC Ensembl
Outerchr5:28657050..28782832hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg38125783
hg19125783
hg18125783
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787878
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894160
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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