A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059425



Internal ID21968658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18708222..18708278hg38UCSC Ensembl
chr20:18688866..18688922hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631340
Samples
Known GenesDTD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059425
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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