A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv987n223



Internal ID22803955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:21358735..21463562hg38UCSC Ensembl
chr11:21380281..21485108hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38104828
hg19104828
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6437627, nsv6438375
Samples
Known GenesNELL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv987n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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