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nsv6837146

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:95

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 110 SVs from 28 studies. See in: genome view    
    Submitted genomic99,034,776-99,034,870Question Mark
    Overlapping variant regions from other studies: 109 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):98,632,399-98,632,493Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6837146Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr799,034,77699,034,870
    nsv6837146RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr798,632,39998,632,493

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18728727duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18728727Submitted genomicNC_000007.14:g.990
    34776_99034870dup
    GRCh38 (hg38)NC_000007.14Chr799,034,77699,034,870
    nssv18728727RemappedPerfectNC_000007.13:g.986
    32399_98632493dup
    GRCh37.p13First PassNC_000007.13Chr798,632,39998,632,493

    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)
    nssv187287274e-061223184
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