A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765893



Internal ID20541753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39405887..39405887hg38UCSC Ensembl
chr14:39875091..39875091hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg382937
hg192937
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293395
Samples
Known GenesFBXO33
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765893
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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