A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5593908



Internal ID21542500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33699054..33701293hg38UCSC Ensembl
chr20:32286860..32289099hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg382240
hg192240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116530
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5593908
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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