A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993854



Internal ID21903197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43054540..43060924hg38UCSC Ensembl
chr3:43096032..43102416hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg386385
hg196385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555704
Samples
Known GenesFAM198A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993854
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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