A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226089



Internal ID20793129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124711626..124712378hg38UCSC Ensembl
chr11:124581522..124582274hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38753
hg19753
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587678
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226089
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