A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027331



Internal ID21936674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108102066..108130451hg38UCSC Ensembl
chr11:107972793..108001178hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3828386
hg1928386
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588105
Samples
Known GenesACAT1, CUL5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027331
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