A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17020563



Internal ID81353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13937639..13937642hg38UCSC Ensembl
chr9:13937638..13937641hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg382676
hg192676
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557205
Supporting Variants
Samples
Known GenesLINC00583
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17020563
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000937


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