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nsv5531231

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:74

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 107 SVs from 17 studies. See in: genome view    
Submitted genomic50,202,029-50,202,102Question Mark
Overlapping variant regions from other studies: 107 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):50,494,226-50,494,299Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5531231Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1550,202,02950,202,102
nsv5531231RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1550,494,22650,494,299

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17703074deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17703074Submitted genomicNC_000015.10:g.502
02029_50202102del
GRCh38 (hg38)NC_000015.10Chr1550,202,02950,202,102
nssv17703074RemappedPerfectNC_000015.9:g.5049
4226_50494299del
GRCh37.p13First PassNC_000015.9Chr1550,494,22650,494,299

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)
nssv17703074<0.00116404
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