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nsv6998773

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,056,901

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 14317 SVs from 116 studies. See in: genome view    
    Submitted genomic44,716,377-50,773,277Question Mark
    Overlapping variant regions from other studies: 14352 SVs from 117 studies. See in: genome view    
    Remapped(Score: Good):42,296,342-48,299,647Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6998773Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1844,716,37750,773,277
    nsv6998773RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1842,296,34248,299,647

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18633878duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18633878Submitted genomicNC_000018.10:g.447
    16377_50773277dup
    GRCh38 (hg38)NC_000018.10Chr1844,716,37750,773,277
    nssv18633878RemappedGoodNC_000018.9:g.4229
    6342_48299647dup
    GRCh37.p13First PassNC_000018.9Chr1842,296,34248,299,647

    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)
    nssv186338784e-061275374
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