A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5942087



Internal ID22717519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:34664443..34958104hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38293662
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386365
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5942087
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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