A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787993



Internal ID18831666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:105632931..105828256hg38UCSC Ensembl
Innerchr11:105503658..105698982hg19UCSC Ensembl
Innerchr11:105008868..105204192hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38195326
hg19195325
hg18195325
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892096
Supporting Variants
Samples
Known GenesGRIA4
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=25
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787993
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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