A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890686



Internal ID18838302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:102222379..102234787hg38UCSC Ensembl
Outerchr5:102222379..102234787hg38UCSC Ensembl
Innerchr5:101558083..101570491hg19UCSC Ensembl
Outerchr5:101558083..101570491hg19UCSC Ensembl
Innerchr5:101585982..101598390hg18UCSC Ensembl
Outerchr5:101585982..101598390hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3812409
hg1912409
hg1812409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797193
Samples
Known GenesSLCO4C1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890686
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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