A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466793



Internal ID21124346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47115616..47120716hg38UCSC Ensembl
chr11:47137167..47142267hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg385101
hg195101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186475
Samples
Known GenesC11orf49
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466793
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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