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nsv7011189

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,372

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 173 SVs from 42 studies. See in: genome view    
    Submitted genomic48,820,233-48,833,604Question Mark
    Overlapping variant regions from other studies: 173 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):49,323,490-49,336,861Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7011189Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1948,820,23348,833,604
    nsv7011189RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1949,323,49049,336,861

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18424039deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18424039Submitted genomicNC_000019.10:g.488
    20233_48833604del
    GRCh38 (hg38)NC_000019.10Chr1948,820,23348,833,604
    nssv18424039RemappedPerfectNC_000019.9:g.4932
    3490_49336861del
    GRCh37.p13First PassNC_000019.9Chr1949,323,49049,336,861

    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)
    nssv18424039<0.00172275788
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