A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235414



Internal ID20802454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22883222..22883708hg38UCSC Ensembl
chr11:22904768..22905254hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38487
hg19487
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594546
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235414
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0004


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