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nsv7004750

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,896

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 212 SVs from 20 studies. See in: genome view    
    Submitted genomic9,564,562-9,568,457Question Mark
    Overlapping variant regions from other studies: 212 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):9,564,560-9,568,455Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7004750Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr189,564,5629,568,457
    nsv7004750RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr189,564,5609,568,455

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18420713deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18420713Submitted genomicNC_000018.10:g.956
    4562_9568457del
    GRCh38 (hg38)NC_000018.10Chr189,564,5629,568,457
    nssv18420713RemappedPerfectNC_000018.9:g.9564
    560_9568455del
    GRCh37.p13First PassNC_000018.9Chr189,564,5609,568,455

    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)
    nssv184207134e-061275382
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