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nsv7069055

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,323,514

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2728 SVs from 85 studies. See in: genome view    
    Submitted genomic37,465,340-38,788,853Question Mark
    Overlapping variant regions from other studies: 2728 SVs from 85 studies. See in: genome view    
    Remapped(Score: Perfect):37,757,541-39,081,054Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7069055Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1537,465,34038,788,853
    nsv7069055RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1537,757,54139,081,054

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18754377inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18754377Submitted genomicNC_000015.10:g.374
    65340_38788853inv
    GRCh38 (hg38)NC_000015.10Chr1537,465,34038,788,853
    nssv18754377RemappedPerfectNC_000015.9:g.3775
    7541_39081054inv
    GRCh37.p13First PassNC_000015.9Chr1537,757,54139,081,054

    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)
    nssv187543774e-061276268
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