A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236930



Internal ID20803970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9403176..9570594hg38UCSC Ensembl
chr12:9555772..9723190hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38167419
hg19167419
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594687
Supporting Variants
Samples
Known GenesDDX12P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236930
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00341


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