A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232749



Internal ID20799789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116968308..116969312hg38UCSC Ensembl
chr11:116839024..116840028hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381005
hg191005
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580371
Supporting Variants
Samples
Known GenesSIK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232749
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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