A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790227



Internal ID19162595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55167087..55592737hg38UCSC Ensembl
Innerchr11:54934563..55360213hg19UCSC Ensembl
Innerchr11:54691139..55116789hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38425651
hg19425651
hg18425651
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892009
Supporting Variants
Samples
Known GenesOR4A15, OR4A16, OR4C15, OR4C16, TRIM48, TRIM51HP
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=60
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790227
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer