A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237893



Internal ID20804933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58345749..58346933hg38UCSC Ensembl
chr14:58812467..58813651hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg381185
hg191185
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586790
Supporting Variants
Samples
Known GenesARID4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237893
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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