A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995182



Internal ID21904525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1372673..1372835hg38UCSC Ensembl
chr4:1366461..1366623hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549971
Samples
Known GenesUVSSA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995182
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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