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nsv6671460

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:19,300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 129 SVs from 24 studies. See in: genome view    
    Submitted genomic68,654,201-68,673,500Question Mark
    Overlapping variant regions from other studies: 129 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):68,881,333-68,900,632Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6671460Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr268,654,20168,673,500
    nsv6671460RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr268,881,33368,900,632

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18669326duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18669326Submitted genomicNC_000002.12:g.686
    54201_68673500dup
    GRCh38 (hg38)NC_000002.12Chr268,654,20168,673,500
    nssv18669326RemappedPerfectNC_000002.11:g.688
    81333_68900632dup
    GRCh37.p13First PassNC_000002.11Chr268,881,33368,900,632

    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)
    nssv186693264e-061275992
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