A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1276n223



Internal ID22804244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94229201..94254400hg38UCSC Ensembl
chr11:93962367..93987566hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3825200
hg1925200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6466273, nsv6462569
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1276n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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