A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5528089



Internal ID304161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11743358..11746960hg38UCSC Ensembl
chr16:11837214..11840816hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg383603
hg193603
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704600
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5528089
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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