A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17594701



Internal ID21786744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:43187082..43187082hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38578
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6086743
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17594701
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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