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nsv4515152

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 46 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):41,998,058-41,998,058Question Mark
Overlapping variant regions from other studies: 46 SVs from 6 studies. See in: genome view    
Submitted genomic42,394,062-42,394,062Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4515152RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000022.11Chr2241,998,05841,998,058
nsv4515152Submitted genomicGRCh37.p13Primary AssemblyNC_000022.10Chr2242,394,06242,394,062

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16036041alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16036041RemappedPerfectNC_000022.11:g.419
98058_41998059ins1
10
GRCh38.p12First PassNC_000022.11Chr2241,998,05841,998,058
nssv16036041Submitted genomicNC_000022.10:g.423
94062_42394063ins1
10
GRCh37.p13NC_000022.10Chr2242,394,06242,394,062

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)
nssv160360414.6e-005121694
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