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nsv6673064

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:374,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1362 SVs from 79 studies. See in: genome view    
    Submitted genomic61,378,101-61,752,800Question Mark
    Overlapping variant regions from other studies: 1362 SVs from 79 studies. See in: genome view    
    Remapped(Score: Perfect):61,605,236-61,979,935Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6673064Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr261,378,10161,752,800
    nsv6673064RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr261,605,23661,979,935

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18665946duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18665946Submitted genomicNC_000002.12:g.613
    78101_61752800dup
    GRCh38 (hg38)NC_000002.12Chr261,378,10161,752,800
    nssv18665946RemappedPerfectNC_000002.11:g.616
    05236_61979935dup
    GRCh37.p13First PassNC_000002.11Chr261,605,23661,979,935

    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)
    nssv186659464e-061275890
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