A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17639832



Internal ID21831879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:46539168..46663032hg38UCSC Ensembl
chr21:47959081..48082944hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38123865
hg19123864
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6048051
Supporting Variants
Samples
Known GenesDIP2A, PRMT2, S100B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17639832
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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