A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011508



Internal ID21920851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111471130..111479722hg38UCSC Ensembl
chr10:113230888..113239480hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg388593
hg198593
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596879
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011508
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