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nsv5557815

  • 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: 92 SVs from 22 studies. See in: genome view    
Submitted genomic47,561,608-47,561,659Question Mark
Overlapping variant regions from other studies: 92 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):47,603,098-47,603,149Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5557815Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr347,561,60847,561,659
nsv5557815RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr347,603,09847,603,149

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16932970sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16932970Submitted genomicNC_000003.12:g.475
61608_47561659ins1
316
GRCh38 (hg38)NC_000003.12Chr347,561,60847,561,659
nssv16932970RemappedPerfectNC_000003.11:g.476
03098_47603149ins1
316
GRCh37.p13First PassNC_000003.11Chr347,603,09847,603,149

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)
nssv16932970<0.00116404
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