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nsv7017789

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:128

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 70 SVs from 20 studies. See in: genome view    
    Submitted genomic51,591,017-51,591,144Question Mark
    Overlapping variant regions from other studies: 70 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):52,094,270-52,094,397Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7017789Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1951,591,01751,591,144
    nsv7017789RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1952,094,27052,094,397

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18638753duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18638753Submitted genomicNC_000019.10:g.515
    91017_51591144dup
    GRCh38 (hg38)NC_000019.10Chr1951,591,01751,591,144
    nssv18638753RemappedPerfectNC_000019.9:g.5209
    4270_52094397dup
    GRCh37.p13First PassNC_000019.9Chr1952,094,27052,094,397

    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)
    nssv186387534e-061226646
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