A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17617879



Internal ID21809926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53522017..53522084hg38UCSC Ensembl
chr20:52138556..52138623hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6051297
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17617879
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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