A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232550



Internal ID20799590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20589395..20589861hg38UCSC Ensembl
chr14:21057554..21058020hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38467
hg19467
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578228
Supporting Variants
Samples
Known GenesRNASE11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232550
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