A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469082



Internal ID21126635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122578958..122640359hg38UCSC Ensembl
chr11:122449666..122511067hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3861402
hg1961402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190684
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469082
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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