A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5634n152



Internal ID22821337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11724478..11726576hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382099
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3220991, nsv3212501
SamplesHG00731, HG00732, HG00733
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)dgv5634n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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