A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16975296



Internal ID50918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159300463..159300467hg38UCSC Ensembl
chr5:158727471..158727475hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5552618
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16975296
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.018576


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