A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893136



Internal ID18837270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:69882369..69887172hg38UCSC Ensembl
Outerchr18:69881391..69889410hg38UCSC Ensembl
Innerchr18:67549605..67554408hg19UCSC Ensembl
Outerchr18:67548627..67556646hg19UCSC Ensembl
Innerchr18:65700585..65705388hg18UCSC Ensembl
Outerchr18:65699607..65707626hg18UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg388020
hg198020
hg188020
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798040, essv25797002, essv25796697, essv25796033, essv25800054, essv25797785
Samples
Known GenesCD226
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893136
Frequency
Sample Size3017
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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