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nsv7073253

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:18,761

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 132 SVs from 27 studies. See in: genome view    
    Submitted genomic88,160,921-88,179,681Question Mark
    Overlapping variant regions from other studies: 132 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):87,894,089-87,912,849Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7073253Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1188,160,92188,179,681
    nsv7073253RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1187,894,08987,912,849

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18741832inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18741832Submitted genomicNC_000011.10:g.881
    60921_88179681inv
    GRCh38 (hg38)NC_000011.10Chr1188,160,92188,179,681
    nssv18741832RemappedPerfectNC_000011.9:g.8789
    4089_87912849inv
    GRCh37.p13First PassNC_000011.9Chr1187,894,08987,912,849

    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)
    nssv187418324e-061276268
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