A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17706559



Internal ID130225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24510294..24510343hg38UCSC Ensembl
chr16:24521615..24521664hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38273
hg19273
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5418722
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17706559
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.010771


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