A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782979



Internal ID19176449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:7686537..7909093hg38UCSC Ensembl
Innerchr11:7707768..7930640hg19UCSC Ensembl
Innerchr11:7664344..7887216hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38222557
hg19222873
hg18222873
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891927
Supporting Variants
Samples
Known GenesLOC283299, OR5E1P, OR5P2, OR5P3, OVCH2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=78
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782979
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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