A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17630119



Internal ID21822166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77334795..77334795hg38UCSC Ensembl
chr16:77368692..77368692hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6093016
Supporting Variants
Samples
Known GenesADAMTS18
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17630119
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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