A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5518975



Internal ID295336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:79857039..79893626hg38UCSC Ensembl
chr16:79890936..79927523hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3836588
hg1936588
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17708307
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5518975
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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