A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464201



Internal ID21121754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134252901..134254100hg38UCSC Ensembl
chr11:134122795..134123994hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988246
Samples
Known GenesACAD8, THYN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464201
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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