A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241189



Internal ID20808229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58995478..58996559hg38UCSC Ensembl
chr15:59287677..59288758hg19UCSC Ensembl
Cytoband15q22.1
Allele length
AssemblyAllele length
hg381082
hg191082
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594160
Supporting Variants
Samples
Known GenesRNF111
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241189
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