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nsv6870811

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,546

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 155 SVs from 40 studies. See in: genome view    
    Submitted genomic92,418,261-92,428,806Question Mark
    Overlapping variant regions from other studies: 155 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):95,180,543-95,191,088Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6870811Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr992,418,26192,428,806
    nsv6870811RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr995,180,54395,191,088

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18589857deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18589857Submitted genomicNC_000009.12:g.924
    18261_92428806del
    GRCh38 (hg38)NC_000009.12Chr992,418,26192,428,806
    nssv18589857RemappedPerfectNC_000009.11:g.951
    80543_95191088del
    GRCh37.p13First PassNC_000009.11Chr995,180,54395,191,088

    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)
    nssv185898572.8e-058275968
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