A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14346780



Internal ID22186560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65522563..65536558hg38UCSC Ensembl
chr9:44799291..44813237hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3813996
hg1913947
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3227592
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14346780
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