A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14355659



Internal ID22141950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91797781..91799876hg38UCSC Ensembl
chr10:93557538..93559633hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg382096
hg192096
Variant TypeCNV duplication
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3218260
Supporting Variants
SamplesHG00513
Known GenesTNKS2, TNKS2-AS1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14355659
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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