A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221012



Internal ID20788052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:41591124..42486420hg38UCSC Ensembl
chr14:42060327..42955623hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38895297
hg19895297
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580548
Supporting Variants
Samples
Known GenesLRFN5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221012
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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