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nsv7040610

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,819,145

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 9289 SVs from 114 studies. See in: genome view    
    Submitted genomic59,230,466-63,049,610Question Mark
    Overlapping variant regions from other studies: 9306 SVs from 114 studies. See in: genome view    
    Remapped(Score: Good):59,216,192-63,035,286Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7040610Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr359,230,46663,049,610
    nsv7040610RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr359,216,19263,035,286

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18772355inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18772355Submitted genomicNC_000003.12:g.592
    30466_63049610inv
    GRCh38 (hg38)NC_000003.12Chr359,230,46663,049,610
    nssv18772355RemappedGoodNC_000003.11:g.592
    16192_63035286inv
    GRCh37.p13First PassNC_000003.11Chr359,216,19263,035,286

    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)
    nssv187723554e-061276268
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