A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14348745



Internal ID22275619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135534367..135534428hg38UCSC Ensembl
chr9:138426213..138426274hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3211176
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14348745
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