A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16938112



Internal ID26139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:124087911..124087962hg38UCSC Ensembl
chr3:123806758..123806809hg19UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5405927
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16938112
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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