A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532195



Internal ID308123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67934909..67934999hg38UCSC Ensembl
chr16:67968812..67968902hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17707539
Samples
Known GenesPSMB10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532195
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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