A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762884



Internal ID20538744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:131311763..131646327hg38UCSC Ensembl
chr12:131796308..132130872hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38334565
hg19334565
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv25n199
Supporting Variantsnssv16269932
Samples
Known GenesLOC338797
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762884
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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