A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv521n209



Internal ID22826596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:24952930..25349536hg38UCSC Ensembl
chr13:25527068..25923674hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38396607
hg19396607
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5975068, nsv5974508
Samples
Known GenesAMER2, MTMR6, NUPL1, PABPC3, TPTE2P1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv521n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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