A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796569



Internal ID18815362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67734155..67964485hg38UCSC Ensembl
Innerchr11:67501626..67731956hg19UCSC Ensembl
Innerchr11:67258202..67488532hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38230331
hg19230331
hg18230331
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892023
Supporting Variants
Samples
Known GenesFAM86C2P
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796569
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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