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nsv6754878

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:648

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 112 SVs from 28 studies. See in: genome view    
    Submitted genomic101,342,069-101,342,716Question Mark
    Overlapping variant regions from other studies: 112 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):102,263,226-102,263,873Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6754878Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4101,342,069101,342,716
    nsv6754878RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4102,263,226102,263,873

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18681621duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18681621Submitted genomicNC_000004.12:g.101
    342069_101342716du
    p
    GRCh38 (hg38)NC_000004.12Chr4101,342,069101,342,716
    nssv18681621RemappedPerfectNC_000004.11:g.102
    263226_102263873du
    p
    GRCh37.p13First PassNC_000004.11Chr4102,263,226102,263,873

    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)
    nssv186816214e-061253846
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