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nsv7013326

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:145,502

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 951 SVs from 70 studies. See in: genome view    
    Submitted genomic53,625,084-53,770,585Question Mark
    Overlapping variant regions from other studies: 952 SVs from 70 studies. See in: genome view    
    Remapped(Score: Perfect):54,128,338-54,273,839Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7013326Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1953,625,08453,770,585
    nsv7013326RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1954,128,33854,273,839

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18639471duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18639471Submitted genomicNC_000019.10:g.536
    25084_53770585dup
    GRCh38 (hg38)NC_000019.10Chr1953,625,08453,770,585
    nssv18639471RemappedPerfectNC_000019.9:g.5412
    8338_54273839dup
    GRCh37.p13First PassNC_000019.9Chr1954,128,33854,273,839

    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)
    nssv186394714e-061273938
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