A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738517



Internal ID162183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104598552..104605300hg38UCSC Ensembl
chr9:107360833..107367581hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg386749
hg196749
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5477955
Supporting Variants
Samples
Known GenesOR13C2, OR13C5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738517
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00692


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