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nsv6704254

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:19,626

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 173 SVs from 35 studies. See in: genome view    
    Submitted genomic16,387,380-16,407,005Question Mark
    Overlapping variant regions from other studies: 173 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):16,428,887-16,448,512Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6704254Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr316,387,38016,407,005
    nsv6704254RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr316,428,88716,448,512

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18671700duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18671700Submitted genomicNC_000003.12:g.163
    87380_16407005dup
    GRCh38 (hg38)NC_000003.12Chr316,387,38016,407,005
    nssv18671700RemappedPerfectNC_000003.11:g.164
    28887_16448512dup
    GRCh37.p13First PassNC_000003.11Chr316,428,88716,448,512

    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)
    nssv186717004e-061276104
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