A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449056



Internal ID227305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189501792..189501878hg38UCSC Ensembl
chr3:189219581..189219667hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16942691
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449056
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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