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nsv7058187

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,807,295

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 11533 SVs from 116 studies. See in: genome view    
    Submitted genomic27,002,297-30,809,591Question Mark
    Overlapping variant regions from other studies: 11533 SVs from 116 studies. See in: genome view    
    Remapped(Score: Perfect):27,291,226-31,098,520Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7058187Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1027,002,29730,809,591
    nsv7058187RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1027,291,22631,098,520

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18732689inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18732689Submitted genomicNC_000010.11:g.270
    02297_30809591inv
    GRCh38 (hg38)NC_000010.11Chr1027,002,29730,809,591
    nssv18732689RemappedPerfectNC_000010.10:g.272
    91226_31098520inv
    GRCh37.p13First PassNC_000010.10Chr1027,291,22631,098,520

    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)
    nssv187326894e-061276268
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