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nsv6668355

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,642

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 114 SVs from 25 studies. See in: genome view    
    Submitted genomic64,997,045-64,998,686Question Mark
    Overlapping variant regions from other studies: 114 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):65,224,179-65,225,820Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6668355Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr264,997,04564,998,686
    nsv6668355RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr265,224,17965,225,820

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18666572duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18666572Submitted genomicNC_000002.12:g.649
    97045_64998686dup
    GRCh38 (hg38)NC_000002.12Chr264,997,04564,998,686
    nssv18666572RemappedPerfectNC_000002.11:g.652
    24179_65225820dup
    GRCh37.p13First PassNC_000002.11Chr265,224,17965,225,820

    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)
    nssv186665727e-062268692
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