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nsv6891679

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,439

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 111 SVs from 23 studies. See in: genome view    
    Submitted genomic11,818,268-11,821,706Question Mark
    Overlapping variant regions from other studies: 111 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):11,860,267-11,863,705Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6891679Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1011,818,26811,821,706
    nsv6891679RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1011,860,26711,863,705

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18332294deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18332294Submitted genomicNC_000010.11:g.118
    18268_11821706del
    GRCh38 (hg38)NC_000010.11Chr1011,818,26811,821,706
    nssv18332294RemappedPerfectNC_000010.10:g.118
    60267_11863705del
    GRCh37.p13First PassNC_000010.10Chr1011,860,26711,863,705

    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)
    nssv183322941.8e-055276218
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