A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235787



Internal ID20802827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:45122795..45123140hg38UCSC Ensembl
chr14:45591998..45592343hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581281
Supporting Variants
Samples
Known GenesFKBP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235787
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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