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nsv7069255

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,520

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 106 SVs from 28 studies. See in: genome view    
    Submitted genomic75,886,103-75,891,622Question Mark
    Overlapping variant regions from other studies: 106 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):77,645,861-77,651,380Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7069255Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1075,886,10375,891,622
    nsv7069255RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1077,645,86177,651,380

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18743203inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18743203Submitted genomicNC_000010.11:g.758
    86103_75891622inv
    GRCh38 (hg38)NC_000010.11Chr1075,886,10375,891,622
    nssv18743203RemappedPerfectNC_000010.10:g.776
    45861_77651380inv
    GRCh37.p13First PassNC_000010.10Chr1077,645,86177,651,380

    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)
    nssv187432034e-061276268
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