A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992147



Internal ID21901490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:176724369..176813567hg38UCSC Ensembl
chr3:176442157..176531355hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3889199
hg1989199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556083
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992147
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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