A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893108



Internal ID19183928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59647575..59656558hg38UCSC Ensembl
Outerchr18:59647575..59656558hg38UCSC Ensembl
Innerchr18:57314807..57323790hg19UCSC Ensembl
Outerchr18:57314807..57323790hg19UCSC Ensembl
Innerchr18:55465787..55474770hg18UCSC Ensembl
Outerchr18:55465787..55474770hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg388984
hg198984
hg188984
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796155
Samples
Known GenesCCBE1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893108
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer