A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16958407



Internal ID39588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169895892..169895943hg38UCSC Ensembl
chr4:170817043..170817094hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554597
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16958407
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.016578


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