A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287890



Internal ID20497108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1403250..1403250hg38UCSC Ensembl
chr20:1383894..1383894hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4766321
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287890
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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