A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225914



Internal ID20792954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92136616..92137891hg38UCSC Ensembl
chr10:93896373..93897648hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg381276
hg191276
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591810
Supporting Variants
Samples
Known GenesCPEB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225914
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