A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796372



Internal ID19167088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:126372802..126378316hg38UCSC Ensembl
Innerchr11:126242697..126248211hg19UCSC Ensembl
Innerchr11:125747907..125753421hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg385515
hg195515
hg185515
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892106
Supporting Variants
Samples
Known GenesST3GAL4
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796372
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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