A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026850



Internal ID21936193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96039667..96040493hg38UCSC Ensembl
chr11:95772831..95773657hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38827
hg19827
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585881
Samples
Known GenesMAML2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026850
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