A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14347530



Internal ID22135476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104493269..104493375hg38UCSC Ensembl
chr9:107255550..107255656hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527418
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14347530
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