A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525853



Internal ID302001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:63764874..63787377hg38UCSC Ensembl
chr16:63798778..63821281hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3822504
hg1922504
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17710066
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525853
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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