A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2190n223



Internal ID22805158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70932017..70932638hg38UCSC Ensembl
chr14:71398734..71399355hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38622
hg19622
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6580650, nsv6586904
Samples
Known GenesPCNX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2190n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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