A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6052519



Internal ID21961752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1259923..1260302hg38UCSC Ensembl
chr20:1240567..1240946hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38380
hg19380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636278
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6052519
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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