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nsv7047492

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,062

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 121 SVs from 31 studies. See in: genome view    
    Submitted genomic47,844,898-47,847,959Question Mark
    Overlapping variant regions from other studies: 121 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):48,310,570-48,313,631Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7047492Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr147,844,89847,847,959
    nsv7047492RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr148,310,57048,313,631

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18761069inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18761069Submitted genomicNC_000001.11:g.478
    44898_47847959inv
    GRCh38 (hg38)NC_000001.11Chr147,844,89847,847,959
    nssv18761069RemappedPerfectNC_000001.10:g.483
    10570_48313631inv
    GRCh37.p13First PassNC_000001.10Chr148,310,57048,313,631

    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)
    nssv187610694e-061276268
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