A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587062



Internal ID20960133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:24419777..24938197hg38UCSC Ensembl
chr13:24993915..25512335hg19UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg38518421
hg19518421
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220956
Samples
Known GenesATP12A, CENPJ, PARP4, RNF17, TPTE2P1, TPTE2P6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587062
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer