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nsv5434230

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:810

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 107 SVs from 22 studies. See in: genome view    
Submitted genomic72,443,541-72,444,350Question Mark
Overlapping variant regions from other studies: 107 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):72,492,692-72,493,501Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5434230Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr372,443,54172,444,350
nsv5434230RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr372,492,69272,493,501

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16935746duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16935746Submitted genomicNC_000003.12:g.724
43541_72444350dup
GRCh38 (hg38)NC_000003.12Chr372,443,54172,444,350
nssv16935746RemappedPerfectNC_000003.11:g.724
92692_72493501dup
GRCh37.p13First PassNC_000003.11Chr372,492,69272,493,501

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)
nssv16935746<0.00116404
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