A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14346784



Internal ID22145528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66253887..66273157hg38UCSC Ensembl
chr9:42248540..42267126hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3819271
hg1918587
Variant TypeCNV duplication
Copy Number57
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3226471
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14346784
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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