A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235582



Internal ID20802622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:70228482..70229065hg38UCSC Ensembl
chr12:70622262..70622845hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg38584
hg19584
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589114
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235582
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