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nsv7054126

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:706,045

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2448 SVs from 90 studies. See in: genome view    
    Submitted genomic87,165,000-87,871,044Question Mark
    Overlapping variant regions from other studies: 2448 SVs from 90 studies. See in: genome view    
    Remapped(Score: Perfect):88,086,152-88,792,196Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7054126Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr487,165,00087,871,044
    nsv7054126RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr488,086,15288,792,196

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18776440inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18776440Submitted genomicNC_000004.12:g.871
    65000_87871044inv
    GRCh38 (hg38)NC_000004.12Chr487,165,00087,871,044
    nssv18776440RemappedPerfectNC_000004.11:g.880
    86152_88792196inv
    GRCh37.p13First PassNC_000004.11Chr488,086,15288,792,196

    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)
    nssv18776440<0.00153269868
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