A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14349680



Internal ID22261746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98238007..98238822hg38UCSC Ensembl
chr9:101000289..101001104hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38816
hg19816
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527395
Supporting Variants
SamplesNA19238
Known GenesTBC1D2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14349680
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