nsv5515791

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:167

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 136 SVs from 20 studies. See in: genome view    
Submitted genomic2,413,439-2,413,605Question Mark
Overlapping variant regions from other studies: 136 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):2,463,440-2,463,606Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5515791Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr162,413,4392,413,605
nsv5515791RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr162,463,4402,463,606

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17706768deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17706768Submitted genomicNC_000016.10:g.241
3439_2413605del
GRCh38 (hg38)NC_000016.10Chr162,413,4392,413,605
nssv17706768RemappedPerfectNC_000016.9:g.2463
440_2463606del
GRCh37.p13First PassNC_000016.9Chr162,463,4402,463,606

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)
nssv17706768<0.00116404
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