A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14369522



Internal ID22205965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58956577..58956644hg38UCSC Ensembl
chr14:59423295..59423362hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3224232
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14369522
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