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nsv7068127

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:72,832

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 352 SVs from 57 studies. See in: genome view    
    Submitted genomic57,850,191-57,923,022Question Mark
    Overlapping variant regions from other studies: 352 SVs from 57 studies. See in: genome view    
    Remapped(Score: Perfect):58,361,559-58,434,390Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7068127Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1957,850,19157,923,022
    nsv7068127RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1958,361,55958,434,390

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18761405inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18761405Submitted genomicNC_000019.10:g.578
    50191_57923022inv
    GRCh38 (hg38)NC_000019.10Chr1957,850,19157,923,022
    nssv18761405RemappedPerfectNC_000019.9:g.5836
    1559_58434390inv
    GRCh37.p13First PassNC_000019.9Chr1958,361,55958,434,390

    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)
    nssv187614054e-061276268
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