A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17688447



Internal ID112113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124016182..124023364hg38UCSC Ensembl
chr11:123886889..123894071hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg387183
hg197183
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5503511
Supporting Variants
Samples
Known GenesOR10G4, OR10G9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17688447
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000469


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