A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv989n223



Internal ID22803957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22046302..22252921hg38UCSC Ensembl
chr11:22067848..22274467hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38206620
hg19206620
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6439784, nsv6440902
Samples
Known GenesANO5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv989n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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