A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv993n223



Internal ID22803961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:23519849..23521425hg38UCSC Ensembl
chr11:23541395..23542971hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg381577
hg191577
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6589810, nsv6595016
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv993n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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