A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1178n223



Internal ID22804146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57985301..57991600hg38UCSC Ensembl
chr11:57752773..57759072hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg386300
hg196300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6463910, nsv6456222
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1178n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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