A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268650



Internal ID20835690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:147865845..147872191hg38UCSC Ensembl
chr5:147245408..147251754hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg386347
hg196347
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566351
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268650
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.05779


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer