A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14374391



Internal ID22194287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:79967919..79973321hg38UCSC Ensembl
chr14:80434262..80439664hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg385403
hg195403
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3241116
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14374391
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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