A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17646676



Internal ID21838723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64318380..64327852hg38UCSC Ensembl
chr20:62949733..62959205hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg389473
hg199473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6044110
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17646676
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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