A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525266



Internal ID301433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69815175..69824788hg38UCSC Ensembl
chr16:69849078..69858691hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg389614
hg199614
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17707145
Samples
Known GenesWWP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525266
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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