A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17709099



Internal ID132765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66545588..66550793hg38UCSC Ensembl
chr16:66579491..66584696hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg385206
hg195206
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563255
Supporting Variants
Samples
Known GenesTK2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17709099
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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