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nsv6923502

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,806

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 122 SVs from 31 studies. See in: genome view    
    Submitted genomic53,468,832-53,471,637Question Mark
    Overlapping variant regions from other studies: 122 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):53,862,616-53,865,421Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6923502Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1253,468,83253,471,637
    nsv6923502RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1253,862,61653,865,421

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18361173deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18361173Submitted genomicNC_000012.12:g.534
    68832_53471637del
    GRCh38 (hg38)NC_000012.12Chr1253,468,83253,471,637
    nssv18361173RemappedPerfectNC_000012.11:g.538
    62616_53865421del
    GRCh37.p13First PassNC_000012.11Chr1253,862,61653,865,421

    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)
    nssv183611734e-061262694
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