A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17591716



Internal ID21783759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:120924580..120924580hg38UCSC Ensembl
chr9:123686858..123686858hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6092962
Supporting Variants
Samples
Known GenesTRAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17591716
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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