A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14345459



Internal ID22217604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17925745..17945766hg38UCSC Ensembl
chr9:17925743..17945764hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3820022
hg1920022
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527934
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14345459
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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