A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891726



Internal ID18839436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:122525151..122556503hg38UCSC Ensembl
Outerchr9:122525151..122556503hg38UCSC Ensembl
Innerchr9:125287430..125318782hg19UCSC Ensembl
Outerchr9:125287430..125318782hg19UCSC Ensembl
Innerchr9:124327251..124358603hg18UCSC Ensembl
Outerchr9:124327251..124358603hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3831353
hg1931353
hg1831353
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796108
Samples
Known GenesOR1N1, OR1N2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891726
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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