A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17709743



Internal ID133409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77334732..77335096hg38UCSC Ensembl
chr16:77368629..77368993hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5532757
Supporting Variants
Samples
Known GenesADAMTS18
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17709743
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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