A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702042



Internal ID15438694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5352021..5352332hg38UCSC Ensembl
Innerchr11:5373251..5373562hg19UCSC Ensembl
Innerchr11:5329827..5330138hg18UCSC Ensembl
Innerchr11:5329827..5330138hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38312
hg19312
hg18312
hg17312
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525848
Supporting Variants
Samples
Known GenesOR51B5, OR51B6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702042
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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