A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782602



Internal ID18818384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55606497..55685447hg38UCSC Ensembl
Innerchr11:55373973..55452923hg19UCSC Ensembl
Innerchr11:55130549..55209499hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3878951
hg1978951
hg1878951
Variant TypeCNV loss
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892006
Supporting Variants
Samples
Known GenesOR4C6, OR4P4, OR4S2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=30
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782602
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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