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nsv6963018

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:351

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 109 SVs from 21 studies. See in: genome view    
    Submitted genomic58,717,433-58,717,783Question Mark
    Overlapping variant regions from other studies: 109 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):59,009,632-59,009,982Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6963018Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1558,717,43358,717,783
    nsv6963018RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1559,009,63259,009,982

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18617489duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18617489Submitted genomicNC_000015.10:g.587
    17433_58717783dup
    GRCh38 (hg38)NC_000015.10Chr1558,717,43358,717,783
    nssv18617489RemappedPerfectNC_000015.9:g.5900
    9632_59009982dup
    GRCh37.p13First PassNC_000015.9Chr1559,009,63259,009,982

    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)
    nssv186174894e-061229564
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