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nsv7068929

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:551,002

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2000 SVs from 94 studies. See in: genome view    
    Submitted genomic42,170,594-42,721,595Question Mark
    Overlapping variant regions from other studies: 2000 SVs from 94 studies. See in: genome view    
    Remapped(Score: Perfect):42,639,797-43,190,798Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7068929Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1442,170,59442,721,595
    nsv7068929RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1442,639,79743,190,798

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18755550inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18755550Submitted genomicNC_000014.9:g.4217
    0594_42721595inv
    GRCh38 (hg38)NC_000014.9Chr1442,170,59442,721,595
    nssv18755550RemappedPerfectNC_000014.8:g.4263
    9797_43190798inv
    GRCh37.p13First PassNC_000014.8Chr1442,639,79743,190,798

    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)
    nssv187555504e-061276268
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