A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463066



Internal ID21120619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125183203..125183479hg38UCSC Ensembl
chr11:125053099..125053375hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987865
Samples
Known GenesPKNOX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463066
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