A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030211



Internal ID21939554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106778240..106784068hg38UCSC Ensembl
chr13:107430588..107436416hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg385829
hg195829
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614000
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030211
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