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nsv7075546

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:390,137

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3979 SVs from 98 studies. See in: genome view    
    Submitted genomic132,775,990-133,166,126Question Mark
    Overlapping variant regions from other studies: 3979 SVs from 98 studies. See in: genome view    
    Remapped(Score: Perfect):134,589,494-134,979,630Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7075546Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10132,775,990133,166,126
    nsv7075546RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10134,589,494134,979,630

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18749691inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18749691Submitted genomicNC_000010.11:g.132
    775990_133166126in
    v
    GRCh38 (hg38)NC_000010.11Chr10132,775,990133,166,126
    nssv18749691RemappedPerfectNC_000010.10:g.134
    589494_134979630in
    v
    GRCh37.p13First PassNC_000010.10Chr10134,589,494134,979,630

    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)
    nssv187496914e-061276266
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