A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17041684



Internal ID95495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5123827..5194475hg38UCSC Ensembl
chr11:5145057..5215705hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3870649
hg1970649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5509825
Supporting Variants
Samples
Known GenesOR52A1, OR52A5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17041684
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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