A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237923



Internal ID20804963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68441344..68831278hg38UCSC Ensembl
chr14:68908061..69297995hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg38389935
hg19389935
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581795
Supporting Variants
Samples
Known GenesRAD51B, ZFP36L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237923
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.01519


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