A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1214n223



Internal ID22804182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66797519..66798608hg38UCSC Ensembl
chr11:66564990..66566079hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg381090
hg191090
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6582598, nsv6593201
Samples
Known GenesC11orf80
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1214n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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