A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16929192



Internal ID20168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16309521..16309521hg38UCSC Ensembl
chr3:16351028..16351028hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5553092
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16929192
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.893014


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