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nsv7004708

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,564

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 107 SVs from 22 studies. See in: genome view    
    Submitted genomic1,468,227-1,478,790Question Mark
    Overlapping variant regions from other studies: 107 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):1,448,872-1,459,435Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7004708Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr201,468,2271,478,790
    nsv7004708RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr201,448,8721,459,435

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18429219deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18429219Submitted genomicNC_000020.11:g.146
    8227_1478790del
    GRCh38 (hg38)NC_000020.11Chr201,468,2271,478,790
    nssv18429219RemappedPerfectNC_000020.10:g.144
    8872_1459435del
    GRCh37.p13First PassNC_000020.10Chr201,448,8721,459,435

    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)
    nssv184292194e-061276062
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