A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14301413



Internal ID22163684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11814471..11829642hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3815172
Variant TypeCNV duplication
Copy Number286
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3218567
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14301413
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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