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nsv6415575

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,079

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 116 SVs from 21 studies. See in: genome view    
    Submitted genomic83,684,739-83,685,817Question Mark
    Overlapping variant regions from other studies: 116 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):84,394,458-84,395,536Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6415575Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr683,684,73983,685,817
    nsv6415575RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr684,394,45884,395,536

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18145918deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18145918Submitted genomicNC_000006.12:g.836
    84739_83685817del
    GRCh38 (hg38)NC_000006.12Chr683,684,73983,685,817
    nssv18145918RemappedPerfectNC_000006.11:g.843
    94458_84395536del
    GRCh37.p13First PassNC_000006.11Chr684,394,45884,395,536

    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)
    nssv18145918<0.0011037926
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