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nsv7077173

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:267,391

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 661 SVs from 59 studies. See in: genome view    
    Submitted genomic96,042,489-96,309,879Question Mark
    Overlapping variant regions from other studies: 661 SVs from 59 studies. See in: genome view    
    Remapped(Score: Perfect):96,508,826-96,776,216Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7077173Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1496,042,48996,309,879
    nsv7077173RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1496,508,82696,776,216

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18755384inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18755384Submitted genomicNC_000014.9:g.9604
    2489_96309879inv
    GRCh38 (hg38)NC_000014.9Chr1496,042,48996,309,879
    nssv18755384RemappedPerfectNC_000014.8:g.9650
    8826_96776216inv
    GRCh37.p13First PassNC_000014.8Chr1496,508,82696,776,216

    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)
    nssv187553844e-061276268
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