A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv930n223



Internal ID22803898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1667189..1683495hg38UCSC Ensembl
chr11:1688419..1704725hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3816307
hg1916307
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6594407, nsv6588417
Samples
Known GenesFAM99A, FAM99B, MOB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv930n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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