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nsv6554550

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:87,156

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 314 SVs from 53 studies. See in: genome view    
    Submitted genomic74,041,572-74,128,727Question Mark
    Overlapping variant regions from other studies: 314 SVs from 53 studies. See in: genome view    
    Remapped(Score: Perfect):74,090,723-74,177,878Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6554550Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr374,041,57274,128,727
    nsv6554550RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr374,090,72374,177,878

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18262947inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18262947Submitted genomicNC_000003.12:g.740
    41572_74128727inv
    GRCh38 (hg38)NC_000003.12Chr374,041,57274,128,727
    nssv18262947RemappedPerfectNC_000003.11:g.740
    90723_74177878inv
    GRCh37.p13First PassNC_000003.11Chr374,090,72374,177,878

    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)
    nssv18262947<0.001139304
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