A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14348305



Internal ID22136868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109356640..109361833hg38UCSC Ensembl
chr9:112118920..112124113hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg385194
hg195194
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527619
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14348305
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