A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17622471



Internal ID21814518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4798547..4798836hg38UCSC Ensembl
chr20:4779193..4779482hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6045581
Supporting Variants
Samples
Known GenesRASSF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17622471
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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