A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238558



Internal ID20805598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:69427027..69428218hg38UCSC Ensembl
chr14:69893744..69894935hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg381192
hg191192
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578873
Supporting Variants
Samples
Known GenesSLC39A9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238558
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