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nsv7069223

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:163,435

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 580 SVs from 56 studies. See in: genome view    
    Submitted genomic95,460,643-95,624,077Question Mark
    Overlapping variant regions from other studies: 580 SVs from 56 studies. See in: genome view    
    Remapped(Score: Perfect):95,926,980-96,090,414Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7069223Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1495,460,64395,624,077
    nsv7069223RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1495,926,98096,090,414

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18755374inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18755374Submitted genomicNC_000014.9:g.9546
    0643_95624077inv
    GRCh38 (hg38)NC_000014.9Chr1495,460,64395,624,077
    nssv18755374RemappedPerfectNC_000014.8:g.9592
    6980_96090414inv
    GRCh37.p13First PassNC_000014.8Chr1495,926,98096,090,414

    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)
    nssv187553744e-061276268
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