A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5592737



Internal ID21541321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:9213104..9213377hg38UCSC Ensembl
chr20:9193751..9194024hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17118055
SamplesNA19239
Known GenesPLCB4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5592737
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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