A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033270



Internal ID21942613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66491219..66508219hg38UCSC Ensembl
chr16:66525122..66542122hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3817001
hg1917001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634571
Samples
Known GenesBEAN1, TK2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033270
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