A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668809



Internal ID21617114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35123879..35157836hg38UCSC Ensembl
chr20:33711682..33745639hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3833958
hg1933958
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116850
Samples
Known GenesEDEM2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668809
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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