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nsv6535509

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,311

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 95 SVs from 28 studies. See in: genome view    
    Submitted genomic58,365,155-58,367,465Question Mark
    Overlapping variant regions from other studies: 95 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):58,876,522-58,878,832Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6535509Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1958,365,15558,367,465
    nsv6535509RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1958,876,52258,878,832

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18049902deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18049902Submitted genomicNC_000019.10:g.583
    65155_58367465del
    GRCh38 (hg38)NC_000019.10Chr1958,365,15558,367,465
    nssv18049902RemappedPerfectNC_000019.9:g.5887
    6522_58878832del
    GRCh37.p13First PassNC_000019.9Chr1958,876,52258,878,832

    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)
    nssv18049902<0.001138894
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