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nsv7061343

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:68,072

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 520 SVs from 72 studies. See in: genome view    
    Submitted genomic12,568,475-12,636,546Question Mark
    Overlapping variant regions from other studies: 520 SVs from 72 studies. See in: genome view    
    Remapped(Score: Perfect):12,679,289-12,747,360Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7061343Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1912,568,47512,636,546
    nsv7061343RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1912,679,28912,747,360

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18757820inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18757820Submitted genomicNC_000019.10:g.125
    68475_12636546inv
    GRCh38 (hg38)NC_000019.10Chr1912,568,47512,636,546
    nssv18757820RemappedPerfectNC_000019.9:g.1267
    9289_12747360inv
    GRCh37.p13First PassNC_000019.9Chr1912,679,28912,747,360

    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)
    nssv187578205.7e-0516273888
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