A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892096



Internal ID18839806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:105632931..105828256hg38UCSC Ensembl
Outerchr11:105632931..105828256hg38UCSC Ensembl
Innerchr11:105503658..105698982hg19UCSC Ensembl
Outerchr11:105503658..105698982hg19UCSC Ensembl
Innerchr11:105008868..105204192hg18UCSC Ensembl
Outerchr11:105008868..105204192hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38195326
hg19195325
hg18195325
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787993
Samples
Known GenesGRIA4
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892096
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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