A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2090n223



Internal ID22805058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:31606166..31607242hg38UCSC Ensembl
chr14:32075372..32076448hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg381077
hg191077
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6580114, nsv6584454
Samples
Known GenesNUBPL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2090n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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