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nsv7054969

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:137,521

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 449 SVs from 59 studies. See in: genome view    
    Submitted genomic13,881,274-14,018,794Question Mark
    Overlapping variant regions from other studies: 449 SVs from 59 studies. See in: genome view    
    Remapped(Score: Perfect):13,881,505-14,019,025Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7054969Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr613,881,27414,018,794
    nsv7054969RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr613,881,50514,019,025

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18780224inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18780224Submitted genomicNC_000006.12:g.138
    81274_14018794inv
    GRCh38 (hg38)NC_000006.12Chr613,881,27414,018,794
    nssv18780224RemappedPerfectNC_000006.11:g.138
    81505_14019025inv
    GRCh37.p13First PassNC_000006.11Chr613,881,50514,019,025

    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)
    nssv187802244e-061276268
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