A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16936442



Internal ID25019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:114793500..114793504hg38UCSC Ensembl
chr3:114512347..114512351hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5408380
Supporting Variants
Samples
Known GenesZBTB20
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16936442
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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