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nsv7040934

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,738

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 112 SVs from 30 studies. See in: genome view    
    Submitted genomic19,603,976-19,609,713Question Mark
    Overlapping variant regions from other studies: 112 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):19,930,470-19,936,207Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7040934Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr119,603,97619,609,713
    nsv7040934RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr119,930,47019,936,207

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18732287inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18732287Submitted genomicNC_000001.11:g.196
    03976_19609713inv
    GRCh38 (hg38)NC_000001.11Chr119,603,97619,609,713
    nssv18732287RemappedPerfectNC_000001.10:g.199
    30470_19936207inv
    GRCh37.p13First PassNC_000001.10Chr119,930,47019,936,207

    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)
    nssv187322871.1e-053275910
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