A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14391113



Internal ID22306382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89204983..89204983hg38UCSC Ensembl
chr14:89671327..89671327hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3560550
Supporting Variants
SamplesNA19240
Known GenesFOXN3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14391113
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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