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nsv7045242

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,922

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 110 SVs from 27 studies. See in: genome view    
    Submitted genomic36,384,890-36,391,811Question Mark
    Overlapping variant regions from other studies: 110 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):36,850,491-36,857,412Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7045242Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr136,384,89036,391,811
    nsv7045242RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr136,850,49136,857,412

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18761531inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18761531Submitted genomicNC_000001.11:g.363
    84890_36391811inv
    GRCh38 (hg38)NC_000001.11Chr136,384,89036,391,811
    nssv18761531RemappedPerfectNC_000001.10:g.368
    50491_36857412inv
    GRCh37.p13First PassNC_000001.10Chr136,850,49136,857,412

    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)
    nssv187615312.5e-057274048
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