A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448842



Internal ID21106395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28276207..28295829hg38UCSC Ensembl
chr11:28297754..28317376hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3819623
hg1919623
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189231
Samples
Known GenesMETTL15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448842
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