A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991675



Internal ID21901018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:152090496..152136502hg38UCSC Ensembl
chr3:151808285..151854291hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3846007
hg1946007
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17542635
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991675
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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