A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591096



Internal ID20964167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:79821755..79823681hg38UCSC Ensembl
chr12:80215535..80217461hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg381927
hg191927
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230346
Samples
Known GenesPPP1R12A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591096
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