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nsv7067412

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:35,327

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 411 SVs from 57 studies. See in: genome view    
    Submitted genomic19,125,661-19,160,987Question Mark
    Overlapping variant regions from other studies: 417 SVs from 58 studies. See in: genome view    
    Remapped(Score: Perfect):19,125,659-19,160,985Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7067412Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr919,125,66119,160,987
    nsv7067412RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr919,125,65919,160,985

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18785791inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18785791Submitted genomicNC_000009.12:g.191
    25661_19160987inv
    GRCh38 (hg38)NC_000009.12Chr919,125,66119,160,987
    nssv18785791RemappedPerfectNC_000009.11:g.191
    25659_19160985inv
    GRCh37.p13First PassNC_000009.11Chr919,125,65919,160,985

    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)
    nssv187857914e-061276266
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