A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1282n223



Internal ID22804250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:97107083..97233147hg38UCSC Ensembl
chr11:96978083..97104147hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38126065
hg19126065
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6458395, nsv6464999
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1282n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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