A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5527707



Internal ID303792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87301656..87359958hg38UCSC Ensembl
chr16:87335262..87393564hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3858303
hg1958303
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17708459
Samples
Known GenesC16orf95, FBXO31
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5527707
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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