A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026886



Internal ID21936229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:50187318..50191970hg38UCSC Ensembl
chr16:50221229..50225881hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg384653
hg194653
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17620885
Samples
Known GenesPAPD5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026886
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer