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nsv7060840

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:142

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 261 SVs from 30 studies. See in: genome view    
    Submitted genomic19,684,238-19,684,379Question Mark
    Overlapping variant regions from other studies: 261 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):19,587,551-19,587,692Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7060840Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1719,684,23819,684,379
    nsv7060840RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1719,587,55119,587,692

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756229inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756229Submitted genomicNC_000017.11:g.196
    84238_19684379inv
    GRCh38 (hg38)NC_000017.11Chr1719,684,23819,684,379
    nssv18756229RemappedPerfectNC_000017.10:g.195
    87551_19587692inv
    GRCh37.p13First PassNC_000017.10Chr1719,587,55119,587,692

    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)
    nssv187562297e-062276206
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