A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024518



Internal ID84080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:79478640..79478678hg38UCSC Ensembl
chr9:82093555..82093593hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5397595
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024518
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.004839


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