A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17555704



Internal ID21880059
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 StatusS
Merged Variantsnsv5993854
Supporting Variants
Samples
Known GenesFAM198A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17555704
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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