A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528103



Internal ID22397487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66166427..66171848hg38UCSC Ensembl
chr11:65933898..65939319hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg385422
hg195422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1428n152
Supporting Variantsnssv14360501, nssv14360502
SamplesNA19239, NA19240
Known GenesPACS1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528103
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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