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nsv7064841

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,801

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 123 SVs from 24 studies. See in: genome view    
    Submitted genomic88,216,026-88,221,826Question Mark
    Overlapping variant regions from other studies: 123 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):88,759,257-88,765,057Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7064841Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1588,216,02688,221,826
    nsv7064841RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1588,759,25788,765,057

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756086inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756086Submitted genomicNC_000015.10:g.882
    16026_88221826inv
    GRCh38 (hg38)NC_000015.10Chr1588,216,02688,221,826
    nssv18756086RemappedPerfectNC_000015.9:g.8875
    9257_88765057inv
    GRCh37.p13First PassNC_000015.9Chr1588,759,25788,765,057

    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)
    nssv187560864e-061276268
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