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nsv6905360

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:280,192

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 999 SVs from 92 studies. See in: genome view    
    Submitted genomic67,712,738-67,992,929Question Mark
    Overlapping variant regions from other studies: 997 SVs from 92 studies. See in: genome view    
    Remapped(Score: Perfect):67,480,209-67,760,400Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6905360Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1167,712,73867,992,929
    nsv6905360RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1167,480,20967,760,400

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18353135deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18353135Submitted genomicNC_000011.10:g.677
    12738_67992929del
    GRCh38 (hg38)NC_000011.10Chr1167,712,73867,992,929
    nssv18353135RemappedPerfectNC_000011.9:g.6748
    0209_67760400del
    GRCh37.p13First PassNC_000011.9Chr1167,480,20967,760,400

    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)
    nssv183531350.002490253100
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