A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992673



Internal ID21902016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187868246..187896185hg38UCSC Ensembl
chr3:187586034..187613973hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3827940
hg1927940
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547594
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992673
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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