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nsv6993665

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,306

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 103 SVs from 23 studies. See in: genome view    
    Submitted genomic27,710,651-27,712,956Question Mark
    Overlapping variant regions from other studies: 103 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):27,721,972-27,724,277Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6993665Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1627,710,65127,712,956
    nsv6993665RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1627,721,97227,724,277

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18400362deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18400362Submitted genomicNC_000016.10:g.277
    10651_27712956del
    GRCh38 (hg38)NC_000016.10Chr1627,710,65127,712,956
    nssv18400362RemappedPerfectNC_000016.9:g.2772
    1972_27724277del
    GRCh37.p13First PassNC_000016.9Chr1627,721,97227,724,277

    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)
    nssv184003627e-062275854
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