A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3218260



Internal ID22363658
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14355658, nssv14355661, nssv14355664, nssv14355663, nssv14355659, nssv14355662, nssv14355665, nssv14355660, nssv14355666
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesTNKS2, TNKS2-AS1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3218260
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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