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nsv7019531

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:566

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 121 SVs from 18 studies. See in: genome view    
    Submitted genomic43,535,522-43,536,087Question Mark
    Overlapping variant regions from other studies: 121 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):42,164,162-42,164,727Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7019531Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2043,535,52243,536,087
    nsv7019531RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2042,164,16242,164,727

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18641465duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18641465Submitted genomicNC_000020.11:g.435
    35522_43536087dup
    GRCh38 (hg38)NC_000020.11Chr2043,535,52243,536,087
    nssv18641465RemappedPerfectNC_000020.10:g.421
    64162_42164727dup
    GRCh37.p13First PassNC_000020.10Chr2042,164,16242,164,727

    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)
    nssv186414654e-061250046
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