A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059017



Internal ID21968250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:6841273..6841334hg38UCSC Ensembl
chr20:6821920..6821981hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621533
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059017
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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