A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518199



Internal ID15445492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:124516115..124580084hg38UCSC Ensembl
Innerchr11:124386011..124449980hg19UCSC Ensembl
Innerchr11:123891221..123955190hg18UCSC Ensembl
Innerchr11:123891221..123955190hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3863970
hg1963970
hg1863970
hg1763970
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695622
Samples
Known GenesOR8A1, OR8B12
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518199
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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