A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17589359



Internal ID21781402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32977146..32977146hg38UCSC Ensembl
chr9:32977144..32977144hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6088960
Supporting Variants
Samples
Known GenesAPTX
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17589359
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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