A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460868



Internal ID21118421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130123901..130193008hg38UCSC Ensembl
chr11:129993796..130062903hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3869108
hg1969108
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183038
Samples
Known GenesAPLP2, ST14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460868
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