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nsv6826002

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:127,727

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 340 SVs from 55 studies. See in: genome view    
    Submitted genomic40,436,195-40,563,921Question Mark
    Overlapping variant regions from other studies: 340 SVs from 55 studies. See in: genome view    
    Remapped(Score: Perfect):40,475,794-40,603,520Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6826002Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr740,436,19540,563,921
    nsv6826002RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr740,475,79440,603,520

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18542081deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18542081Submitted genomicNC_000007.14:g.404
    36195_40563921del
    GRCh38 (hg38)NC_000007.14Chr740,436,19540,563,921
    nssv18542081RemappedPerfectNC_000007.13:g.404
    75794_40603520del
    GRCh37.p13First PassNC_000007.13Chr740,475,79440,603,520

    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)
    nssv185420811.1e-053274874
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