A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529373



Internal ID22398765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62143053..62143212hg38UCSC Ensembl
chr11:61910525..61910684hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14359747, nssv14359752, nssv14359745, nssv14359748, nssv14359744, nssv14359750, nssv14359746, nssv14359749, nssv14359751
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesINCENP
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529373
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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