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nsv7061986

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:86,339

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 271 SVs from 51 studies. See in: genome view    
    Submitted genomic20,392,856-20,479,194Question Mark
    Overlapping variant regions from other studies: 271 SVs from 51 studies. See in: genome view    
    Remapped(Score: Perfect):20,414,402-20,500,740Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7061986Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1120,392,85620,479,194
    nsv7061986RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1120,414,40220,500,740

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18740043inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18740043Submitted genomicNC_000011.10:g.203
    92856_20479194inv
    GRCh38 (hg38)NC_000011.10Chr1120,392,85620,479,194
    nssv18740043RemappedPerfectNC_000011.9:g.2041
    4402_20500740inv
    GRCh37.p13First PassNC_000011.9Chr1120,414,40220,500,740

    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)
    nssv187400434e-061276268
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