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nsv6525521

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,693

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 99 SVs from 29 studies. See in: genome view    
    Submitted genomic58,359,203-58,361,895Question Mark
    Overlapping variant regions from other studies: 99 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):58,870,569-58,873,261Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6525521Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1958,359,20358,361,895
    nsv6525521RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1958,870,56958,873,261

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18049899deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18049899Submitted genomicNC_000019.10:g.583
    59203_58361895del
    GRCh38 (hg38)NC_000019.10Chr1958,359,20358,361,895
    nssv18049899RemappedPerfectNC_000019.9:g.5887
    0569_58873261del
    GRCh37.p13First PassNC_000019.9Chr1958,870,56958,873,261

    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)
    nssv18049899<0.001138356
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