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nsv7050581

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,181

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 101 SVs from 28 studies. See in: genome view    
    Submitted genomic33,926,027-33,935,207Question Mark
    Overlapping variant regions from other studies: 101 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):34,391,628-34,400,808Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7050581Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr133,926,02733,935,207
    nsv7050581RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr134,391,62834,400,808

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18760315inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18760315Submitted genomicNC_000001.11:g.339
    26027_33935207inv
    GRCh38 (hg38)NC_000001.11Chr133,926,02733,935,207
    nssv18760315RemappedPerfectNC_000001.10:g.343
    91628_34400808inv
    GRCh37.p13First PassNC_000001.10Chr134,391,62834,400,808

    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)
    nssv187603154e-061276268
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