A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17708466



Internal ID132132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87384704..87384868hg38UCSC Ensembl
chr16:87418310..87418474hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5518810
Supporting Variants
Samples
Known GenesFBXO31
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17708466
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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