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nsv6968314

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:36,466

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 166 SVs from 34 studies. See in: genome view    
    Submitted genomic65,340,636-65,377,101Question Mark
    Overlapping variant regions from other studies: 166 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):65,632,974-65,669,439Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6968314Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1565,340,63665,377,101
    nsv6968314RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1565,632,97465,669,439

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18618254duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18618254Submitted genomicNC_000015.10:g.653
    40636_65377101dup
    GRCh38 (hg38)NC_000015.10Chr1565,340,63665,377,101
    nssv18618254RemappedPerfectNC_000015.9:g.6563
    2974_65669439dup
    GRCh37.p13First PassNC_000015.9Chr1565,632,97465,669,439

    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)
    nssv186182544e-061276032
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