A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277536



Internal ID20844576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:24976197..26190585hg38UCSC Ensembl
chr8:24833711..26048101hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg381214389
hg191214391
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568691
Supporting Variants
Samples
Known GenesCDCA2, DOCK5, EBF2, GNRH1, KCTD9, MIR6876
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277536
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