A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5430n152



Internal ID22821133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9614294..9614351hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3290538, nsv3291879
SamplesHG00733, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv5430n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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