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nsv7061137

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:301,068

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3355 SVs from 97 studies. See in: genome view    
    Submitted genomic132,930,727-133,231,794Question Mark
    Overlapping variant regions from other studies: 3355 SVs from 97 studies. See in: genome view    
    Remapped(Score: Perfect):134,744,231-135,045,298Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7061137Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10132,930,727133,231,794
    nsv7061137RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10134,744,231135,045,298

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18736444inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18736444Submitted genomicNC_000010.11:g.132
    930727_133231794in
    v
    GRCh38 (hg38)NC_000010.11Chr10132,930,727133,231,794
    nssv18736444RemappedPerfectNC_000010.10:g.134
    744231_135045298in
    v
    GRCh37.p13First PassNC_000010.10Chr10134,744,231135,045,298

    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)
    nssv187364441.1e-052275936
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