A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024202



Internal ID21933545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62816871..62817987hg38UCSC Ensembl
chr11:62584343..62585459hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381117
hg191117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594678
Samples
Known GenesSTX5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024202
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