A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17041608



Internal ID95443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4332000..4540000hg38UCSC Ensembl
chr11:4353230..4561230hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38208001
hg19208001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5507349
Supporting Variants
Samples
Known GenesOR52B4, OR52K1, OR52K2, TRIM21
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17041608
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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