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nsv6362400

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:827

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 102 SVs from 27 studies. See in: genome view    
    Submitted genomic58,163,945-58,164,771Question Mark
    Overlapping variant regions from other studies: 102 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):58,149,672-58,150,498Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6362400Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr358,163,94558,164,771
    nsv6362400RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr358,149,67258,150,498

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18102928deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18102928Submitted genomicNC_000003.12:g.581
    63945_58164771del
    GRCh38 (hg38)NC_000003.12Chr358,163,94558,164,771
    nssv18102928RemappedPerfectNC_000003.11:g.581
    49672_58150498del
    GRCh37.p13First PassNC_000003.11Chr358,149,67258,150,498

    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)
    nssv18102928<0.0011036784
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