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nsv5414360

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 122 SVs from 24 studies. See in: genome view    
Submitted genomic18,491,627-18,491,678Question Mark
Overlapping variant regions from other studies: 122 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):18,472,271-18,472,322Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5414360Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2018,491,62718,491,678
nsv5414360RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2018,472,27118,472,322

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17731368alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17731368Submitted genomicNC_000020.11:g.184
91627_18491678ins2
81
GRCh38 (hg38)NC_000020.11Chr2018,491,62718,491,678
nssv17731368RemappedPerfectNC_000020.10:g.184
72271_18472322ins2
81
GRCh37.p13First PassNC_000020.10Chr2018,472,27118,472,322

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv177313680.002146404
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