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nsv7062604

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:84

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 117 SVs from 21 studies. See in: genome view    
    Submitted genomic20,665,183-20,665,266Question Mark
    Overlapping variant regions from other studies: 117 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):21,239,322-21,239,405Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7062604Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1320,665,18320,665,266
    nsv7062604RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1321,239,32221,239,405

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18752836inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18752836Submitted genomicNC_000013.11:g.206
    65183_20665266inv
    GRCh38 (hg38)NC_000013.11Chr1320,665,18320,665,266
    nssv18752836RemappedPerfectNC_000013.10:g.212
    39322_21239405inv
    GRCh37.p13First PassNC_000013.10Chr1321,239,32221,239,405

    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)
    nssv187528364e-061276268
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