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nsv7065580

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,187,317

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 29382 SVs from 122 studies. See in: genome view    
    Submitted genomic11,963,576-20,150,892Question Mark
    Overlapping variant regions from other studies: 28995 SVs from 122 studies. See in: genome view    
    Remapped(Score: Good):12,074,391-20,193,556Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7065580Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1911,963,57620,150,892
    nsv7065580RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1912,074,39120,193,556

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18757809inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18757809Submitted genomicNC_000019.10:g.119
    63576_20150892inv
    GRCh38 (hg38)NC_000019.10Chr1911,963,57620,150,892
    nssv18757809RemappedGoodNC_000019.9:g.1207
    4391_20193556inv
    GRCh37.p13First PassNC_000019.9Chr1912,074,39120,193,556

    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)
    nssv187578097e-062276268
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