A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1579n152



Internal ID22817282
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 Variants
Supporting Variantsnsv3216514, nsv3223710
SamplesHG00732, HG00733
Known GenesUSP28
MethodMerging
Sequencing
AnalysisMultiple analysis algorthms
PhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformIllumina HiSeq
See merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv1579n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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