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nsv7065857

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,127

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 118 SVs from 20 studies. See in: genome view    
    Submitted genomic88,106,805-88,109,931Question Mark
    Overlapping variant regions from other studies: 118 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):88,650,036-88,653,162Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7065857Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1588,106,80588,109,931
    nsv7065857RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1588,650,03688,653,162

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756083inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756083Submitted genomicNC_000015.10:g.881
    06805_88109931inv
    GRCh38 (hg38)NC_000015.10Chr1588,106,80588,109,931
    nssv18756083RemappedPerfectNC_000015.9:g.8865
    0036_88653162inv
    GRCh37.p13First PassNC_000015.9Chr1588,650,03688,653,162

    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)
    nssv187560831.1e-053272142
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