A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1205n223



Internal ID22804173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62363678..62385395hg38UCSC Ensembl
chr11:62131150..62152867hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3821718
hg1921718
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6467088, nsv6456822
Samples
Known GenesASRGL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1205n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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