A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796108



Internal ID18814450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:122525151..122556503hg38UCSC Ensembl
Innerchr9:125287430..125318782hg19UCSC Ensembl
Innerchr9:124327251..124358603hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3831353
hg1931353
hg1831353
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891726
Supporting Variants
Samples
Known GenesOR1N1, OR1N2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=19
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796108
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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