A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17590382



Internal ID21782425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:43140849..43140849hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3878
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6089844
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17590382
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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