A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1012n223



Internal ID22803980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27747094..27748111hg38UCSC Ensembl
chr11:27768641..27769658hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg381018
hg191018
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6592279, nsv6576638
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1012n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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