A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228492



Internal ID20795532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124792710..124793692hg38UCSC Ensembl
chr10:126481279..126482261hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38983
hg19983
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576710
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228492
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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