A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17707175



Internal ID130841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:70154111..70155096hg38UCSC Ensembl
chr16:70188014..70188999hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38986
hg19986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522628
Supporting Variants
Samples
Known GenesPDPR
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17707175
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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