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nsv6912067

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:27,983

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 140 SVs from 31 studies. See in: genome view    
    Submitted genomic75,387,213-75,415,195Question Mark
    Overlapping variant regions from other studies: 140 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):75,098,257-75,126,239Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6912067Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1175,387,21375,415,195
    nsv6912067RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1175,098,25775,126,239

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18578235duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18578235Submitted genomicNC_000011.10:g.753
    87213_75415195dup
    GRCh38 (hg38)NC_000011.10Chr1175,387,21375,415,195
    nssv18578235RemappedPerfectNC_000011.9:g.7509
    8257_75126239dup
    GRCh37.p13First PassNC_000011.9Chr1175,098,25775,126,239

    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)
    nssv185782354e-061272268
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