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nsv7075171

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:187,529

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 623 SVs from 61 studies. See in: genome view    
    Submitted genomic16,344,428-16,531,956Question Mark
    Overlapping variant regions from other studies: 623 SVs from 61 studies. See in: genome view    
    Remapped(Score: Perfect):16,386,427-16,573,955Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7075171Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1016,344,42816,531,956
    nsv7075171RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1016,386,42716,573,955

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18732746inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18732746Submitted genomicNC_000010.11:g.163
    44428_16531956inv
    GRCh38 (hg38)NC_000010.11Chr1016,344,42816,531,956
    nssv18732746RemappedPerfectNC_000010.10:g.163
    86427_16573955inv
    GRCh37.p13First PassNC_000010.10Chr1016,386,42716,573,955

    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)
    nssv187327461.8e-055272442
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