A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17707503



Internal ID131169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67473684..67491477hg38UCSC Ensembl
chr16:67507587..67525380hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3817794
hg1917794
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5531662
Supporting Variants
Samples
Known GenesAGRP, ATP6V0D1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17707503
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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