A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997452



Internal ID21906795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:44809044..44830117hg38UCSC Ensembl
chr4:44811061..44832134hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3821074
hg1921074
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551099
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997452
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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