A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040129



Internal ID21949472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58537278..58537366hg38UCSC Ensembl
chr11:58304751..58304839hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580767
Samples
Known GenesLPXN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040129
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