A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468659



Internal ID21126212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112470060..112509624hg38UCSC Ensembl
chr11:112340783..112380347hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3839565
hg1939565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986803
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468659
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