A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2185n223



Internal ID22805153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:67731366..67732127hg38UCSC Ensembl
chr14:68198083..68198844hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg38762
hg19762
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6585790, nsv6589828
Samples
Known GenesRDH12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2185n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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