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nsv7011126

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,053

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 199 SVs from 44 studies. See in: genome view    
    Submitted genomic53,750,963-53,758,015Question Mark
    Overlapping variant regions from other studies: 200 SVs from 44 studies. See in: genome view    
    Remapped(Score: Perfect):54,254,217-54,261,269Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7011126Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1953,750,96353,758,015
    nsv7011126RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1954,254,21754,261,269

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18639485duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18639485Submitted genomicNC_000019.10:g.537
    50963_53758015dup
    GRCh38 (hg38)NC_000019.10Chr1953,750,96353,758,015
    nssv18639485RemappedPerfectNC_000019.9:g.5425
    4217_54261269dup
    GRCh37.p13First PassNC_000019.9Chr1954,254,21754,261,269

    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)
    nssv186394854e-061274988
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