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nsv6992367

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,954

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 173 SVs from 30 studies. See in: genome view    
    Submitted genomic3,434,280-3,440,233Question Mark
    Overlapping variant regions from other studies: 173 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):3,337,574-3,343,527Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6992367Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr173,434,2803,440,233
    nsv6992367RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr173,337,5743,343,527

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18406965deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18406965Submitted genomicNC_000017.11:g.343
    4280_3440233del
    GRCh38 (hg38)NC_000017.11Chr173,434,2803,440,233
    nssv18406965RemappedPerfectNC_000017.10:g.333
    7574_3343527del
    GRCh37.p13First PassNC_000017.10Chr173,337,5743,343,527

    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)
    nssv184069654e-060276206
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