A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797193



Internal ID18825960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:102222379..102234787hg38UCSC Ensembl
Innerchr5:101558083..101570491hg19UCSC Ensembl
Innerchr5:101585982..101598390hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3812409
hg1912409
hg1812409
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890686
Supporting Variants
Samples
Known GenesSLCO4C1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797193
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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