A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937249



Internal ID25545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105959164..105959535hg38UCSC Ensembl
chr3:105678011..105678382hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5448446
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937249
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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