A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17022141



Internal ID82425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:29786266..29846743hg38UCSC Ensembl
chr9:29786264..29846741hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3860478
hg1960478
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5473957
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17022141
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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