A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1742n223



Internal ID22804710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:131289324..131677863hg38UCSC Ensembl
chr12:131773869..132162408hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38388540
hg19388540
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6581383, nsv6586746, nsv6588582, nsv6587118, nsv6589500, nsv6577064, nsv6582872
Samples
Known GenesLOC338797
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1742n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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