A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17019094



Internal ID80358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14459741..14459778hg38UCSC Ensembl
chr9:14459739..14459776hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5548866
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17019094
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003746


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