A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5998309



Internal ID21907652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:67339718..67350428hg38UCSC Ensembl
chr4:68205436..68216146hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3810711
hg1910711
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549289
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5998309
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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