A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268513



Internal ID20835553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112351172..112366475hg38UCSC Ensembl
chr6:112672374..112687677hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3815304
hg1915304
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556803
Supporting Variants
Samples
Known GenesRFPL4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268513
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