A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16938546



Internal ID26428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:110895595..110895595hg38UCSC Ensembl
chr3:110614442..110614442hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5542436
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16938546
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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