A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469862



Internal ID21127415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63595251..63596249hg38UCSC Ensembl
chr11:63362723..63363721hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38999
hg19999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187691
Samples
Known GenesPLA2G16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469862
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