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nsv7060471

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,070,641

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 21239 SVs from 122 studies. See in: genome view    
    Submitted genomic54,671,401-63,742,041Question Mark
    Overlapping variant regions from other studies: 21241 SVs from 122 studies. See in: genome view    
    Remapped(Score: Perfect):55,138,119-64,208,759Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7060471Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1454,671,40163,742,041
    nsv7060471RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1455,138,11964,208,759

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18754334inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18754334Submitted genomicNC_000014.9:g.5467
    1401_63742041inv
    GRCh38 (hg38)NC_000014.9Chr1454,671,40163,742,041
    nssv18754334RemappedPerfectNC_000014.8:g.5513
    8119_64208759inv
    GRCh37.p13First PassNC_000014.8Chr1455,138,11964,208,759

    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)
    nssv187543344e-061276268
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