A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533421



Internal ID309311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29386486..29434443hg38UCSC Ensembl
chr16:29397807..29445764hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3847958
hg1947958
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17708054
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533421
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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