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nsv7013108

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:193,334

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1173 SVs from 94 studies. See in: genome view    
    Submitted genomic53,254,604-53,447,937Question Mark
    Overlapping variant regions from other studies: 1173 SVs from 94 studies. See in: genome view    
    Remapped(Score: Perfect):53,757,857-53,951,190Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7013108Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1953,254,60453,447,937
    nsv7013108RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1953,757,85753,951,190

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18426121deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18426121Submitted genomicNC_000019.10:g.532
    54604_53447937del
    GRCh38 (hg38)NC_000019.10Chr1953,254,60453,447,937
    nssv18426121RemappedPerfectNC_000019.9:g.5375
    7857_53951190del
    GRCh37.p13First PassNC_000019.9Chr1953,757,85753,951,190

    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)
    nssv184261214e-061274690
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