A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17083899



Internal ID21435636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39405879..39405879hg38UCSC Ensembl
chr14:39875083..39875083hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg382991
hg192991
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5664310
Supporting Variants
SamplesHG00731
Known GenesFBXO33
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17083899
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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