A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797002



Internal ID18835924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:69881391..69889410hg38UCSC Ensembl
Innerchr18:67548627..67556646hg19UCSC Ensembl
Innerchr18:65699607..65707626hg18UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg388020
hg198020
hg188020
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=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797002
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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