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nsv4334316

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:215,720

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 159 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):58,150,575-58,366,294Question Mark
Overlapping variant regions from other studies: 159 SVs from 18 studies. See in: genome view    
Submitted genomic57,918,047-58,133,767Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4334316RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1158,150,57558,366,294
nsv4334316Submitted genomicGRCh37.p13Primary AssemblyNC_000011.9Chr1157,918,04758,133,767

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15787568sequence alterationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv15787568RemappedPerfectGRCh38.p12First PassNC_000011.10Chr1158,150,57558,366,294
nssv15787568Submitted genomicGRCh37.p13NC_000011.9Chr1157,918,04758,133,767

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)
nssv157875689.2e-005221694
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