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nsv5411562

  • 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: 193 SVs from 29 studies. See in: genome view    
Submitted genomic27,181,067-27,181,118Question Mark
Overlapping variant regions from other studies: 199 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):27,181,065-27,181,116Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5411562Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr927,181,06727,181,118
nsv5411562RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr927,181,06527,181,116

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17020177alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17020177Submitted genomicNC_000009.12:g.271
81067_27181118ins2
52
GRCh38 (hg38)NC_000009.12Chr927,181,06727,181,118
nssv17020177RemappedPerfectNC_000009.11:g.271
81065_27181116ins2
52
GRCh37.p13First PassNC_000009.11Chr927,181,06527,181,116

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)
nssv17020177<0.00116404
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