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nsv7005777

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,573

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 207 SVs from 39 studies. See in: genome view    
    Submitted genomic48,831,717-48,837,289Question Mark
    Overlapping variant regions from other studies: 207 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):49,334,974-49,340,546Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7005777Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1948,831,71748,837,289
    nsv7005777RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1949,334,97449,340,546

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18424041deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18424041Submitted genomicNC_000019.10:g.488
    31717_48837289del
    GRCh38 (hg38)NC_000019.10Chr1948,831,71748,837,289
    nssv18424041RemappedPerfectNC_000019.9:g.4933
    4974_49340546del
    GRCh37.p13First PassNC_000019.9Chr1949,334,97449,340,546

    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)
    nssv184240411.5e-054267206
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