A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789530



Internal ID18819841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55600413..55679951hg38UCSC Ensembl
Innerchr11:55367889..55447427hg19UCSC Ensembl
Innerchr11:55124465..55204003hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3879539
hg1979539
hg1879539
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892006
Supporting Variants
Samples
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=29
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789530
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