A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023529



Internal ID83404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33470941..33470989hg38UCSC Ensembl
chr9:33470939..33470987hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5552234
Supporting Variants
Samples
Known GenesNOL6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023529
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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