A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745158



Internal ID20521163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:52248857..52249475hg38UCSC Ensembl
chr16:52282769..52283387hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38619
hg19619
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281026
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745158
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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