A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5632n152



Internal ID22821335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11547399..11554787hg38UCSC Ensembl
chrUn_gl000232:62..7450hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg387389
hg197389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3227346, nsv3214175
SamplesHG00512, NA19238, NA19239, HG00732, NA19240, 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)dgv5632n152
Frequency
Sample Size9
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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