A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5448446



Internal ID226722
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 StatusM
Merged Variants
Supporting Variantsnssv16937249
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5448446
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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