A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003363



Internal ID21912706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:60518561..60527334hg38UCSC Ensembl
chr9_gl000199_random:3..8776hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg388774
hg198774
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583816
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003363
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