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nsv6748280

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 154 SVs from 30 studies. See in: genome view    
    Submitted genomic84,960,601-84,966,600Question Mark
    Overlapping variant regions from other studies: 154 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):85,881,754-85,887,753Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6748280Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr484,960,60184,966,600
    nsv6748280RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr485,881,75485,887,753

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18691107duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18691107Submitted genomicNC_000004.12:g.849
    60601_84966600dup
    GRCh38 (hg38)NC_000004.12Chr484,960,60184,966,600
    nssv18691107RemappedPerfectNC_000004.11:g.858
    81754_85887753dup
    GRCh37.p13First PassNC_000004.11Chr485,881,75485,887,753

    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)
    nssv186911077e-062273266
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