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nsv6449173

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:576

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 76 SVs from 14 studies. See in: genome view    
    Submitted genomic94,080,149-94,080,724Question Mark
    Overlapping variant regions from other studies: 76 SVs from 14 studies. See in: genome view    
    Remapped(Score: Perfect):95,839,906-95,840,481Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6449173Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1094,080,14994,080,724
    nsv6449173RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1095,839,90695,840,481

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17985236deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17985236Submitted genomicNC_000010.11:g.940
    80149_94080724del
    GRCh38 (hg38)NC_000010.11Chr1094,080,14994,080,724
    nssv17985236RemappedPerfectNC_000010.10:g.958
    39906_95840481del
    GRCh37.p13First PassNC_000010.10Chr1095,839,90695,840,481

    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)
    nssv17985236<0.0011438394
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