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nsv7057559

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,889

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 112 SVs from 26 studies. See in: genome view    
    Submitted genomic63,950,930-63,966,818Question Mark
    Overlapping variant regions from other studies: 112 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):63,936,606-63,952,494Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7057559Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr363,950,93063,966,818
    nsv7057559RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr363,936,60663,952,494

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18771739inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18771739Submitted genomicNC_000003.12:g.639
    50930_63966818inv
    GRCh38 (hg38)NC_000003.12Chr363,950,93063,966,818
    nssv18771739RemappedPerfectNC_000003.11:g.639
    36606_63952494inv
    GRCh37.p13First PassNC_000003.11Chr363,936,60663,952,494

    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)
    nssv187717394e-061276268
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