A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993388



Internal ID21902731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45133447..45133743hg38UCSC Ensembl
chr3:45174939..45175235hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551596
Samples
Known GenesCDCP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993388
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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