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nsv5531243

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:395,189

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1300 SVs from 85 studies. See in: genome view    
Submitted genomic82,069,175-82,464,363Question Mark
Overlapping variant regions from other studies: 1300 SVs from 85 studies. See in: genome view    
Remapped(Score: Perfect):82,102,780-82,497,968Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5531243Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1682,069,17582,464,363
nsv5531243RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1682,102,78082,497,968

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17709889duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17709889Submitted genomicNC_000016.10:g.820
69175_82464363dup
GRCh38 (hg38)NC_000016.10Chr1682,069,17582,464,363
nssv17709889RemappedPerfectNC_000016.9:g.8210
2780_82497968dup
GRCh37.p13First PassNC_000016.9Chr1682,102,78082,497,968

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)
nssv17709889<0.00116404
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