A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17648678



Internal ID21840725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:16290589..16296351hg38UCSC Ensembl
chr21:17662910..17668672hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg385763
hg195763
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6047374
Supporting Variants
Samples
Known GenesLINC00478
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17648678
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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