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nsv6713249

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:18,483

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 149 SVs from 38 studies. See in: genome view    
    Submitted genomic32,942,344-32,960,826Question Mark
    Overlapping variant regions from other studies: 149 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):32,983,836-33,002,318Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6713249Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr332,942,34432,960,826
    nsv6713249RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr332,983,83633,002,318

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18678221duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18678221Submitted genomicNC_000003.12:g.329
    42344_32960826dup
    GRCh38 (hg38)NC_000003.12Chr332,942,34432,960,826
    nssv18678221RemappedPerfectNC_000003.11:g.329
    83836_33002318dup
    GRCh37.p13First PassNC_000003.11Chr332,983,83633,002,318

    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)
    nssv186782214e-061275842
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