A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17555989



Internal ID21880344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:159496751..159950843hg38UCSC Ensembl
chr4:160417903..160871995hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38454093
hg19454093
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5995749
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17555989
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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