A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997329



Internal ID21906672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:45220926..45258506hg38UCSC Ensembl
chr4:45222943..45260523hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3837581
hg1937581
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551022
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997329
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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