A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533476



Internal ID309366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68621593..68654708hg38UCSC Ensembl
chr16:68655496..68688611hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3833116
hg1933116
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17708500
Samples
Known GenesCDH3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533476
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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