A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232093



Internal ID20799133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119507609..119509425hg38UCSC Ensembl
chr10:121267121..121268937hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg381817
hg191817
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580074
Supporting Variants
Samples
Known GenesRGS10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232093
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