A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17043168



Internal ID96486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5464000..5676000hg38UCSC Ensembl
chr11:5485230..5697230hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38212001
hg19212001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5506878
Supporting Variants
Samples
Known GenesOR51B5, OR52B6, OR52D1, OR52H1, TRIM34, TRIM5, TRIM6, TRIM6-TRIM34, UBQLN3, UBQLNL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17043168
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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