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nsv7077361

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:70,697

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 335 SVs from 46 studies. See in: genome view    
    Submitted genomic73,582,934-73,653,630Question Mark
    Overlapping variant regions from other studies: 335 SVs from 46 studies. See in: genome view    
    Remapped(Score: Perfect):73,616,833-73,687,529Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7077361Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1673,582,93473,653,630
    nsv7077361RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1673,616,83373,687,529

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18758260inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18758260Submitted genomicNC_000016.10:g.735
    82934_73653630inv
    GRCh38 (hg38)NC_000016.10Chr1673,582,93473,653,630
    nssv18758260RemappedPerfectNC_000016.9:g.7361
    6833_73687529inv
    GRCh37.p13First PassNC_000016.9Chr1673,616,83373,687,529

    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)
    nssv187582600.012795274200
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