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nsv7010519

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,634

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 190 SVs from 22 studies. See in: genome view    
    Submitted genomic47,051,943-47,058,576Question Mark
    Overlapping variant regions from other studies: 190 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):44,578,314-44,584,947Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7010519Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1847,051,94347,058,576
    nsv7010519RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1844,578,31444,584,947

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18418186deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18418186Submitted genomicNC_000018.10:g.470
    51943_47058576del
    GRCh38 (hg38)NC_000018.10Chr1847,051,94347,058,576
    nssv18418186RemappedPerfectNC_000018.9:g.4457
    8314_44584947del
    GRCh37.p13First PassNC_000018.9Chr1844,578,31444,584,947

    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)
    nssv184181864e-061276196
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