A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997025



Internal ID21906368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:34901226..34977139hg38UCSC Ensembl
chr4:34902848..34978761hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3875914
hg1975914
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546417
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997025
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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