A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796155



Internal ID19177975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59647575..59656558hg38UCSC Ensembl
Innerchr18:57314807..57323790hg19UCSC Ensembl
Innerchr18:55465787..55474770hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg388984
hg198984
hg188984
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893108
Supporting Variants
Samples
Known GenesCCBE1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796155
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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