A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16933154



Internal ID22829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65037597..65037648hg38UCSC Ensembl
chr3:65023272..65023323hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5412214
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16933154
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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