A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17019096



Internal ID80360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14480375..14480426hg38UCSC Ensembl
chr9:14480373..14480424hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5412922
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17019096
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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