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nsv7015894

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,176

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 176 SVs from 41 studies. See in: genome view    
    Submitted genomic53,744,310-53,749,485Question Mark
    Overlapping variant regions from other studies: 176 SVs from 41 studies. See in: genome view    
    Remapped(Score: Perfect):54,247,564-54,252,739Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7015894Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1953,744,31053,749,485
    nsv7015894RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1954,247,56454,252,739

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18639484duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18639484Submitted genomicNC_000019.10:g.537
    44310_53749485dup
    GRCh38 (hg38)NC_000019.10Chr1953,744,31053,749,485
    nssv18639484RemappedPerfectNC_000019.9:g.5424
    7564_54252739dup
    GRCh37.p13First PassNC_000019.9Chr1954,247,56454,252,739

    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)
    nssv186394842.9e-058272854
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