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nsv7067666

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,700,288

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 7887 SVs from 117 studies. See in: genome view    
    Submitted genomic19,858,996-21,559,283Question Mark
    Overlapping variant regions from other studies: 7873 SVs from 117 studies. See in: genome view    
    Remapped(Score: Good):19,969,805-21,742,085Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7067666Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1919,858,99621,559,283
    nsv7067666RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1919,969,80521,742,085

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18758535inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18758535Submitted genomicNC_000019.10:g.198
    58996_21559283inv
    GRCh38 (hg38)NC_000019.10Chr1919,858,99621,559,283
    nssv18758535RemappedGoodNC_000019.9:g.1996
    9805_21742085inv
    GRCh37.p13First PassNC_000019.9Chr1919,969,80521,742,085

    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)
    nssv187585354e-061276268
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