A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17621614



Internal ID21813661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21198899..21198899hg38UCSC Ensembl
chr20:21179538..21179538hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6102669
Supporting Variants
Samples
Known GenesPLK1S1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17621614
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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