A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037680



Internal ID21947023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3454300..3454380hg38UCSC Ensembl
chr16:3504300..3504380hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606986
Samples
Known GenesNAA60
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037680
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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