A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894182



Internal ID19185251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:41229175..41234906hg38UCSC Ensembl
Outerchr5:41229175..41234906hg38UCSC Ensembl
Innerchr5:41229277..41235008hg19UCSC Ensembl
Outerchr5:41229277..41235008hg19UCSC Ensembl
Innerchr5:41265034..41270765hg18UCSC Ensembl
Outerchr5:41265034..41270765hg18UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg385732
hg195732
hg185732
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783998, essv25783116, essv25784271, essv25780839, essv25780904, essv25782450, essv25781176, essv25782827, essv25781708, essv25784259, essv25783552, essv25780468, essv25799960, essv25780274
Samples
Known GenesC6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894182
Frequency
Sample Size3017
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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