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nsv6991432

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,579

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 176 SVs from 34 studies. See in: genome view    
    Submitted genomic4,319,319-4,324,897Question Mark
    Overlapping variant regions from other studies: 176 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):4,222,614-4,228,192Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6991432Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr174,319,3194,324,897
    nsv6991432RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr174,222,6144,228,192

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18411448deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18411448Submitted genomicNC_000017.11:g.431
    9319_4324897del
    GRCh38 (hg38)NC_000017.11Chr174,319,3194,324,897
    nssv18411448RemappedPerfectNC_000017.10:g.422
    2614_4228192del
    GRCh37.p13First PassNC_000017.10Chr174,222,6144,228,192

    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)
    nssv184114484e-061276168
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