A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5702n152



Internal ID22821405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27325111..27325227hg38UCSC Ensembl
chr22:27721072..27721188hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3214281, nsv3221854
SamplesHG00512, HG00731, HG00733, 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)dgv5702n152
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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