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nsv7076174

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,701,418

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 17026 SVs from 125 studies. See in: genome view    
    Submitted genomic57,437,573-64,138,990Question Mark
    Overlapping variant regions from other studies: 17026 SVs from 125 studies. See in: genome view    
    Remapped(Score: Perfect):57,205,046-63,906,462Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7076174Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1157,437,57364,138,990
    nsv7076174RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1157,205,04663,906,462

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18738400inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18738400Submitted genomicNC_000011.10:g.574
    37573_64138990inv
    GRCh38 (hg38)NC_000011.10Chr1157,437,57364,138,990
    nssv18738400RemappedPerfectNC_000011.9:g.5720
    5046_63906462inv
    GRCh37.p13First PassNC_000011.9Chr1157,205,04663,906,462

    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)
    nssv187384004e-061276266
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