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nsv7068651

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,495

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 174 SVs from 21 studies. See in: genome view    
    Submitted genomic56,060,428-56,063,922Question Mark
    Overlapping variant regions from other studies: 174 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):53,727,659-53,731,153Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7068651Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1856,060,42856,063,922
    nsv7068651RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1853,727,65953,731,153

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18759777inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18759777Submitted genomicNC_000018.10:g.560
    60428_56063922inv
    GRCh38 (hg38)NC_000018.10Chr1856,060,42856,063,922
    nssv18759777RemappedPerfectNC_000018.9:g.5372
    7659_53731153inv
    GRCh37.p13First PassNC_000018.9Chr1853,727,65953,731,153

    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)
    nssv187597774e-061276268
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