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nsv7060715

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:767

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 258 SVs from 40 studies. See in: genome view    
    Submitted genomic19,315,002-19,315,768Question Mark
    Overlapping variant regions from other studies: 264 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):19,315,000-19,315,766Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7060715Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr919,315,00219,315,768
    nsv7060715RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr919,315,00019,315,766

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18784778inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18784778Submitted genomicNC_000009.12:g.193
    15002_19315768inv
    GRCh38 (hg38)NC_000009.12Chr919,315,00219,315,768
    nssv18784778RemappedPerfectNC_000009.11:g.193
    15000_19315766inv
    GRCh37.p13First PassNC_000009.11Chr919,315,00019,315,766

    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)
    nssv187847780.001289266008
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