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nsv6522457

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,345

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 136 SVs from 23 studies. See in: genome view    
    Submitted genomic55,399,324-55,409,668Question Mark
    Overlapping variant regions from other studies: 135 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):53,476,685-53,487,029Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6522457Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1755,399,32455,409,668
    nsv6522457RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1753,476,68553,487,029

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18036923deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18036923Submitted genomicNC_000017.11:g.553
    99324_55409668del
    GRCh38 (hg38)NC_000017.11Chr1755,399,32455,409,668
    nssv18036923RemappedPerfectNC_000017.10:g.534
    76685_53487029del
    GRCh37.p13First PassNC_000017.10Chr1753,476,68553,487,029

    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)
    nssv18036923<0.001239246
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