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nsv6999449

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:20,195

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 182 SVs from 49 studies. See in: genome view    
    Submitted genomic48,677,031-48,697,225Question Mark
    Overlapping variant regions from other studies: 182 SVs from 49 studies. See in: genome view    
    Remapped(Score: Perfect):49,180,288-49,200,482Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6999449Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1948,677,03148,697,225
    nsv6999449RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1949,180,28849,200,482

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18424020deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18424020Submitted genomicNC_000019.10:g.486
    77031_48697225del
    GRCh38 (hg38)NC_000019.10Chr1948,677,03148,697,225
    nssv18424020RemappedPerfectNC_000019.9:g.4918
    0288_49200482del
    GRCh37.p13First PassNC_000019.9Chr1949,180,28849,200,482

    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)
    nssv184240203.5e-058276188
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