A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518225



Internal ID15098832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55404201..55641224hg38UCSC Ensembl
Innerchr11:55171677..55408700hg19UCSC Ensembl
Innerchr11:54928253..55165276hg18UCSC Ensembl
Innerchr11:54928253..55165276hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38237024
hg19237024
hg18237024
hg17237024
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695649
Samples
Known GenesOR4C11, OR4C15, OR4C16, OR4P4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518225
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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