A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997828



Internal ID21907171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6003426..6004302hg38UCSC Ensembl
chr4:6005153..6006029hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38877
hg19877
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17541480
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997828
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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