A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1779n223



Internal ID22804747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:24580561..25013183hg38UCSC Ensembl
chr13:25154699..25587321hg19UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg38432623
hg19432623
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6591359, nsv6587226, nsv6594018, nsv6589951, nsv6595379
Samples
Known GenesATP12A, CENPJ, RNF17, TPTE2P1, TPTE2P6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1779n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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