A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040257



Internal ID21949600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69182888..69183154hg38UCSC Ensembl
chr11:68950356..68950622hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590312
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040257
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