A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14348814



Internal ID22192649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90106395..90106480hg38UCSC Ensembl
chr9:92868677..92868762hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527951
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14348814
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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