A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223540



Internal ID20790580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:119248350..119249063hg38UCSC Ensembl
chr12:119686155..119686868hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg38714
hg19714
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577031
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223540
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