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nsv6931954

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:563,318

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1715 SVs from 84 studies. See in: genome view    
    Submitted genomic23,439,649-24,002,966Question Mark
    Overlapping variant regions from other studies: 1715 SVs from 84 studies. See in: genome view    
    Remapped(Score: Perfect):24,013,788-24,577,105Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6931954Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1323,439,64924,002,966
    nsv6931954RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1324,013,78824,577,105

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18600046duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18600046Submitted genomicNC_000013.11:g.234
    39649_24002966dup
    GRCh38 (hg38)NC_000013.11Chr1323,439,64924,002,966
    nssv18600046RemappedPerfectNC_000013.10:g.240
    13788_24577105dup
    GRCh37.p13First PassNC_000013.10Chr1324,013,78824,577,105

    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)
    nssv186000461.1e-053275510
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