A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6054421



Internal ID21963654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5268309..5280792hg38UCSC Ensembl
chr20:5248955..5261438hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3812484
hg1912484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636422
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6054421
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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