A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3023n152



Internal ID22818726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90819208..90819350hg38UCSC Ensembl
chr15:91362438..91362580hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3285130, nsv3530008
SamplesHG00732, HG00733, HG00513, HG00514
Known Genes
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)dgv3023n152
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer