A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797243



Internal ID18818897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:111208771..111269737hg38UCSC Ensembl
Innerchr11:111079495..111140462hg19UCSC Ensembl
Innerchr11:110584705..110645672hg18UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3860967
hg1960968
hg1860968
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892101
Supporting Variants
Samples
Known GenesC11orf53
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=18
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797243
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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