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nsv5407726

  • 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: 134 SVs from 23 studies. See in: genome view    
Submitted genomic18,167,894-18,167,945Question Mark
Overlapping variant regions from other studies: 134 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):18,169,517-18,169,568Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5407726Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr418,167,89418,167,945
nsv5407726RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr418,169,51718,169,568

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16948328alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16948328Submitted genomicNC_000004.12:g.181
67894_18167945ins2
80
GRCh38 (hg38)NC_000004.12Chr418,167,89418,167,945
nssv16948328RemappedPerfectNC_000004.11:g.181
69517_18169568ins2
80
GRCh37.p13First PassNC_000004.11Chr418,169,51718,169,568

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)
nssv169483280.003216404
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