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nsv6824934

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:703,680

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1587 SVs from 81 studies. See in: genome view    
    Submitted genomic85,995,444-86,699,123Question Mark
    Overlapping variant regions from other studies: 1587 SVs from 81 studies. See in: genome view    
    Remapped(Score: Perfect):85,624,760-86,328,439Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6824934Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr785,995,44486,699,123
    nsv6824934RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr785,624,76086,328,439

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18547254deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18547254Submitted genomicNC_000007.14:g.859
    95444_86699123del
    GRCh38 (hg38)NC_000007.14Chr785,995,44486,699,123
    nssv18547254RemappedPerfectNC_000007.13:g.856
    24760_86328439del
    GRCh37.p13First PassNC_000007.13Chr785,624,76086,328,439

    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)
    nssv185472544e-061275908
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