A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5516955



Internal ID293393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:90020213..90097273hg38UCSC Ensembl
chr16:90086621..90163681hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3877061
hg1977061
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17708939
Samples
Known GenesC16orf3, GAS8, PRDM7, URAHP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5516955
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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