A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039299



Internal ID21948642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109265506..109270683hg38UCSC Ensembl
chr13:109917854..109923031hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg385178
hg195178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17599435
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039299
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