A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1202n223



Internal ID22804170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60609601..60626800hg38UCSC Ensembl
chr11:60377074..60394273hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3817200
hg1917200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6457245, nsv6459354
Samples
Known GenesLINC00301
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1202n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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