A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3216514



Internal ID22362486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113842640..113861211hg38UCSC Ensembl
chr11:113713362..113731933hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3818572
hg1918572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1579n152
Supporting Variantsnssv14361565, nssv14361564
SamplesHG00732, HG00733
Known GenesUSP28
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3216514
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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