A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234855



Internal ID20801895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:111667699..111668819hg38UCSC Ensembl
chr12:112105503..112106623hg19UCSC Ensembl
Cytoband12q24.12
Allele length
AssemblyAllele length
hg381121
hg191121
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582503
Supporting Variants
Samples
Known GenesBRAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234855
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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