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nsv7063904

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,691,992

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 6451 SVs from 108 studies. See in: genome view    
    Submitted genomic54,352,554-57,044,545Question Mark
    Overlapping variant regions from other studies: 6451 SVs from 108 studies. See in: genome view    
    Remapped(Score: Perfect):54,386,466-57,078,457Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7063904Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1654,352,55457,044,545
    nsv7063904RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1654,386,46657,078,457

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18757574inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18757574Submitted genomicNC_000016.10:g.543
    52554_57044545inv
    GRCh38 (hg38)NC_000016.10Chr1654,352,55457,044,545
    nssv18757574RemappedPerfectNC_000016.9:g.5438
    6466_57078457inv
    GRCh37.p13First PassNC_000016.9Chr1654,386,46657,078,457

    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)
    nssv187575744e-061276268
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