A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14348804



Internal ID22137296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89483670..89483734hg38UCSC Ensembl
chr9:92098585..92098649hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527183
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14348804
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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