A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024668



Internal ID84180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36483394..36483441hg38UCSC Ensembl
chr9:36483391..36483438hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5549808
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024668
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.012332


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