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nsv6971511

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:37,689

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 165 SVs from 34 studies. See in: genome view    
    Submitted genomic72,162,956-72,200,644Question Mark
    Overlapping variant regions from other studies: 165 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):72,455,297-72,492,985Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6971511Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1572,162,95672,200,644
    nsv6971511RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1572,455,29772,492,985

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18619817duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18619817Submitted genomicNC_000015.10:g.721
    62956_72200644dup
    GRCh38 (hg38)NC_000015.10Chr1572,162,95672,200,644
    nssv18619817RemappedPerfectNC_000015.9:g.7245
    5297_72492985dup
    GRCh37.p13First PassNC_000015.9Chr1572,455,29772,492,985

    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)
    nssv186198174e-061275076
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