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nsv6908684

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:279,929

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 992 SVs from 91 studies. See in: genome view    
    Submitted genomic67,708,412-67,988,340Question Mark
    Overlapping variant regions from other studies: 990 SVs from 91 studies. See in: genome view    
    Remapped(Score: Perfect):67,475,883-67,755,811Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6908684Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1167,708,41267,988,340
    nsv6908684RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1167,475,88367,755,811

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18353133deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18353133Submitted genomicNC_000011.10:g.677
    08412_67988340del
    GRCh38 (hg38)NC_000011.10Chr1167,708,41267,988,340
    nssv18353133RemappedPerfectNC_000011.9:g.6747
    5883_67755811del
    GRCh37.p13First PassNC_000011.9Chr1167,475,88367,755,811

    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)
    nssv183531330.002506254168
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