A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057350



Internal ID21966583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63942238..63942297hg38UCSC Ensembl
chr20:62573591..62573650hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17647049
Samples
Known GenesUCKL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057350
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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