A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16938796



Internal ID26590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139405230..139405230hg38UCSC Ensembl
chr3:139124072..139124072hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556264
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16938796
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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