A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3019n152



Internal ID22818722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89325034..89325233hg38UCSC Ensembl
chr15:89868265..89868464hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3528658, nsv3287457, nsv3287098
SamplesHG00512, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesPOLG
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)dgv3019n152
Frequency
Sample Size9
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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