A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790711



Internal ID18831787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:89850051..90149401hg38UCSC Ensembl
Innerchr11:89583219..89882569hg19UCSC Ensembl
Innerchr11:89222867..89522217hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38299351
hg19299351
hg18299351
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892056
Supporting Variants
Samples
Known GenesMIR5692A1, NAALAD2, TRIM49C, TRIM49D1, TRIM49D2P, TRIM53AP, TRIM64, TRIM64B, UBTFL1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=62
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790711
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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