A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288058



Internal ID20497276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50666188..50666188hg38UCSC Ensembl
chr20:49282725..49282725hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4767986
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288058
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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