A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225868



Internal ID20792908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:125898234..125899312hg38UCSC Ensembl
chr12:126382780..126383858hg19UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg381079
hg191079
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577685
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225868
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