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nsv6997293

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,881

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 197 SVs from 30 studies. See in: genome view    
    Submitted genomic58,921,989-58,937,869Question Mark
    Overlapping variant regions from other studies: 196 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):56,999,350-57,015,230Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6997293Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1758,921,98958,937,869
    nsv6997293RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1756,999,35057,015,230

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18413172deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18413172Submitted genomicNC_000017.11:g.589
    21989_58937869del
    GRCh38 (hg38)NC_000017.11Chr1758,921,98958,937,869
    nssv18413172RemappedPerfectNC_000017.10:g.569
    99350_57015230del
    GRCh37.p13First PassNC_000017.10Chr1756,999,35057,015,230

    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)
    nssv18413172<0.001116253340
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