A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14369360



Internal ID22283218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23925343..23925396hg38UCSC Ensembl
chr14:24394552..24394605hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529507
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14369360
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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