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nsv6409393

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:392,145

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1466 SVs from 90 studies. See in: genome view    
    Submitted genomic99,597,024-99,989,168Question Mark
    Overlapping variant regions from other studies: 1466 SVs from 90 studies. See in: genome view    
    Remapped(Score: Perfect):98,932,728-99,324,872Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6409393Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr599,597,02499,989,168
    nsv6409393RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr598,932,72899,324,872

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18136337deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18136337Submitted genomicNC_000005.10:g.995
    97024_99989168del
    GRCh38 (hg38)NC_000005.10Chr599,597,02499,989,168
    nssv18136337RemappedPerfectNC_000005.9:g.9893
    2728_99324872del
    GRCh37.p13First PassNC_000005.9Chr598,932,72899,324,872

    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)
    nssv18136337<0.001138970
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