A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17708476



Internal ID132142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87543938..87564070hg38UCSC Ensembl
chr16:87577544..87597676hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3820133
hg1920133
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5532662
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17708476
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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