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nsv6704243

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,826

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 165 SVs from 33 studies. See in: genome view    
    Submitted genomic9,926,979-9,935,804Question Mark
    Overlapping variant regions from other studies: 165 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):9,968,663-9,977,488Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6704243Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr39,926,9799,935,804
    nsv6704243RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr39,968,6639,977,488

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18681473duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18681473Submitted genomicNC_000003.12:g.992
    6979_9935804dup
    GRCh38 (hg38)NC_000003.12Chr39,926,9799,935,804
    nssv18681473RemappedPerfectNC_000003.11:g.996
    8663_9977488dup
    GRCh37.p13First PassNC_000003.11Chr39,968,6639,977,488

    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)
    nssv186814731.1e-053273398
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