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nsv5499036

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,800

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 117 SVs from 24 studies. See in: genome view    
Submitted genomic43,819,598-43,822,397Question Mark
Overlapping variant regions from other studies: 117 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):44,111,796-44,114,595Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5499036Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1543,819,59843,822,397
nsv5499036RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1544,111,79644,114,595

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17702965deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17702965Submitted genomicNC_000015.10:g.438
19598_43822397del
GRCh38 (hg38)NC_000015.10Chr1543,819,59843,822,397
nssv17702965RemappedPerfectNC_000015.9:g.4411
1796_44114595del
GRCh37.p13First PassNC_000015.9Chr1544,111,79644,114,595

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)
nssv17702965<0.00126404
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