A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17629390



Internal ID21821437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24778413..24778498hg38UCSC Ensembl
chr20:24759049..24759134hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6060130
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17629390
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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