A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221307



Internal ID20788347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:112129035..112129220hg38UCSC Ensembl
chr12:112566839..112567024hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588282
Supporting Variants
Samples
Known GenesTRAFD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221307
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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