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nsv7064398

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:501,392

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1137 SVs from 75 studies. See in: genome view    
    Submitted genomic62,881,040-63,382,431Question Mark
    Overlapping variant regions from other studies: 1137 SVs from 75 studies. See in: genome view    
    Remapped(Score: Perfect):62,648,512-63,149,903Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7064398Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1162,881,04063,382,431
    nsv7064398RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1162,648,51263,149,903

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18734984inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18734984Submitted genomicNC_000011.10:g.628
    81040_63382431inv
    GRCh38 (hg38)NC_000011.10Chr1162,881,04063,382,431
    nssv18734984RemappedPerfectNC_000011.9:g.6264
    8512_63149903inv
    GRCh37.p13First PassNC_000011.9Chr1162,648,51263,149,903

    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)
    nssv187349844e-061276268
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