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nsv6643352

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:147,002

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 386 SVs from 57 studies. See in: genome view    
    Submitted genomic160,655,832-160,802,833Question Mark
    Overlapping variant regions from other studies: 390 SVs from 57 studies. See in: genome view    
    Remapped(Score: Perfect):160,625,622-160,772,623Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6643352Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1160,655,832160,802,833
    nsv6643352RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1160,625,622160,772,623

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18588474duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18588474Submitted genomicNC_000001.11:g.160
    655832_160802833du
    p
    GRCh38 (hg38)NC_000001.11Chr1160,655,832160,802,833
    nssv18588474RemappedPerfectNC_000001.10:g.160
    625622_160772623du
    p
    GRCh37.p13First PassNC_000001.10Chr1160,625,622160,772,623

    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)
    nssv185884744e-061275652
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