A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089560



Internal ID21998793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:48859167..48859167hg38UCSC Ensembl
chr13:49433303..49433303hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg385964
hg195964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617468
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089560
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