A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16932148



Internal ID22156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31468042..31468045hg38UCSC Ensembl
chr3:31509534..31509537hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5402443
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16932148
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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