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nsv7057713

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,169,795

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3033 SVs from 95 studies. See in: genome view    
    Submitted genomic56,332,234-57,502,028Question Mark
    Overlapping variant regions from other studies: 3471 SVs from 97 studies. See in: genome view    
    Remapped(Score: Good):56,197,032-57,366,927Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7057713Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr656,332,23457,502,028
    nsv7057713RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr656,197,03257,366,927

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18779841inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18779841Submitted genomicNC_000006.12:g.563
    32234_57502028inv
    GRCh38 (hg38)NC_000006.12Chr656,332,23457,502,028
    nssv18779841RemappedGoodNC_000006.11:g.561
    97032_57366927inv
    GRCh37.p13First PassNC_000006.11Chr656,197,03257,366,927

    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)
    nssv187798417e-062276268
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