A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1332n223



Internal ID22804300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126237128..126238213hg38UCSC Ensembl
chr11:126107023..126108108hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg381086
hg191086
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6584288, nsv6585377
Samples
Known GenesFAM118B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1332n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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