A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3231472



Internal ID22372244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:46896485..46916160hg38UCSC Ensembl
chr12:47290268..47309943hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg3819676
hg1919676
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1832n152
Supporting Variantsnssv14463465
SamplesHG00732
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3231472
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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