A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459788



Internal ID21117341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68484887..68512584hg38UCSC Ensembl
chr11:68252355..68280052hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3827698
hg1927698
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178246
Samples
Known GenesPPP6R3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459788
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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