A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17633748



Internal ID21825795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60649275..60649275hg38UCSC Ensembl
chr20:59224333..59224333hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6109990
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17633748
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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