A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17596372



Internal ID21788415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128472132..128472132hg38UCSC Ensembl
chr9:131234411..131234411hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6081886
Supporting Variants
Samples
Known GenesODF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17596372
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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