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nsv6889484

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:522,695

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1718 SVs from 88 studies. See in: genome view    
    Submitted genomic4,436,481-4,959,175Question Mark
    Overlapping variant regions from other studies: 1705 SVs from 87 studies. See in: genome view    
    Remapped(Score: Perfect):4,478,673-5,001,367Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6889484Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr104,436,4814,959,175
    nsv6889484RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr104,478,6735,001,367

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18589339duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18589339Submitted genomicNC_000010.11:g.443
    6481_4959175dup
    GRCh38 (hg38)NC_000010.11Chr104,436,4814,959,175
    nssv18589339RemappedPerfectNC_000010.10:g.447
    8673_5001367dup
    GRCh37.p13First PassNC_000010.10Chr104,478,6735,001,367

    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)
    nssv185893394e-061274320
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