A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892106



Internal ID19186502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:126372802..126378316hg38UCSC Ensembl
Outerchr11:126372802..126378316hg38UCSC Ensembl
Innerchr11:126242697..126248211hg19UCSC Ensembl
Outerchr11:126242697..126248211hg19UCSC Ensembl
Innerchr11:125747907..125753421hg18UCSC Ensembl
Outerchr11:125747907..125753421hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg385515
hg195515
hg185515
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797565, essv25796372
Samples
Known GenesST3GAL4
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892106
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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