A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464810



Internal ID21122363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62763569..62765081hg38UCSC Ensembl
chr11:62531041..62532553hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381513
hg191513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993232
Samples
Known GenesPOLR2G
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464810
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