A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17053684



Internal ID103631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124332483..124404353hg38UCSC Ensembl
chr11:124202379..124274249hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3871871
hg1971871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513210
Supporting Variants
Samples
Known GenesOR8B2, OR8B3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17053684
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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