A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17542156



Internal ID21866511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:121607377..121607483hg38UCSC Ensembl
chr3:121326224..121326330hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5991475
Supporting Variants
Samples
Known GenesFBXO40
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17542156
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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