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nsv6966308

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:31,667

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 303 SVs from 59 studies. See in: genome view    
    Submitted genomic87,925,162-87,956,828Question Mark
    Overlapping variant regions from other studies: 303 SVs from 59 studies. See in: genome view    
    Remapped(Score: Perfect):88,391,506-88,423,172Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6966308Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1487,925,16287,956,828
    nsv6966308RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1488,391,50688,423,172

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18391929deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18391929Submitted genomicNC_000014.9:g.8792
    5162_87956828del
    GRCh38 (hg38)NC_000014.9Chr1487,925,16287,956,828
    nssv18391929RemappedPerfectNC_000014.8:g.8839
    1506_88423172del
    GRCh37.p13First PassNC_000014.8Chr1488,391,50688,423,172

    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)
    nssv18391929<0.001155275580
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