A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020551



Internal ID21929894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1225688..1238837hg38UCSC Ensembl
chr16:1275688..1288838hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3813150
hg1913151
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607089
Samples
Known GenesTPSB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020551
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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