A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277855



Internal ID20487073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:303213..303213hg38UCSC Ensembl
chr20:283857..283857hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg382420
hg192420
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4767261
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277855
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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