A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239010



Internal ID20806050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42636894..42637320hg38UCSC Ensembl
chr15:42929092..42929518hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38427
hg19427
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580352
Supporting Variants
Samples
Known GenesSTARD9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239010
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