A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv25n199



Internal ID22802911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:131310490..131647595hg38UCSC Ensembl
chr12:131795035..132132140hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38337106
hg19337106
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4762884, nsv4755350
Samples
Known GenesLOC338797
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)dgv25n199
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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