A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796916



Internal ID18825922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:94211379..94316021hg38UCSC Ensembl
Innerchr11:93944545..94049187hg19UCSC Ensembl
Innerchr11:93584193..93688835hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38104643
hg19104643
hg18104643
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892069
Supporting Variants
Samples
Known GenesFOLR4
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=16
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796916
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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