A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1595n152



Internal ID22817298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119290386..119290979hg38UCSC Ensembl
chr11:119161096..119161689hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38594
hg19594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3226271, nsv3219365
SamplesHG00512, NA19239, HG00732, NA19240, HG00733
Known GenesCBL
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)dgv1595n152
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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