A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589951



Internal ID20963022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:24612703..25013183hg38UCSC Ensembl
chr13:25186841..25587321hg19UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg38400481
hg19400481
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1779n223
Supporting Variantsnssv18219434
Samples
Known GenesATP12A, CENPJ, RNF17, TPTE2P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589951
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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