A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238341



Internal ID20805381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41436819..41439906hg38UCSC Ensembl
chr15:41729017..41732104hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg383088
hg193088
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592788
Supporting Variants
Samples
Known GenesRTF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238341
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