A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3241116



Internal ID22374881
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14374391, nssv14385318
SamplesHG00731, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3241116
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer