A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459406



Internal ID21116959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133354101..133511500hg38UCSC Ensembl
chr11:133223996..133381395hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38157400
hg19157400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194576
Samples
Known GenesOPCML
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459406
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer