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nsv7068131

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,431

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 84 SVs from 20 studies. See in: genome view    
    Submitted genomic91,418,628-91,420,058Question Mark
    Overlapping variant regions from other studies: 84 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):93,178,385-93,179,815Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7068131Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1091,418,62891,420,058
    nsv7068131RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1093,178,38593,179,815

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18749627inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18749627Submitted genomicNC_000010.11:g.914
    18628_91420058inv
    GRCh38 (hg38)NC_000010.11Chr1091,418,62891,420,058
    nssv18749627RemappedPerfectNC_000010.10:g.931
    78385_93179815inv
    GRCh37.p13First PassNC_000010.10Chr1093,178,38593,179,815

    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)
    nssv187496274e-061276266
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