A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1811n223



Internal ID22804779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41236098..41237258hg38UCSC Ensembl
chr13:41810234..41811394hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg381161
hg191161
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6593099, nsv6588357, nsv6589946
Samples
Known GenesMTRF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1811n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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