A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460918



Internal ID21118471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:114638519..114675750hg38UCSC Ensembl
chr11:114509241..114546472hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3837232
hg1937232
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177593
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460918
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