A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796697



Internal ID18820752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:69881391..69887172hg38UCSC Ensembl
Innerchr18:67548627..67554408hg19UCSC Ensembl
Innerchr18:65699607..65705388hg18UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg385782
hg195782
hg185782
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893136
Supporting Variants
Samples
Known GenesCD226
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796697
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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