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nsv7063889

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,222,228

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4216 SVs from 84 studies. See in: genome view    
    Submitted genomic17,856,052-19,078,279Question Mark
    Overlapping variant regions from other studies: 4217 SVs from 84 studies. See in: genome view    
    Remapped(Score: Perfect):17,966,861-19,189,088Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7063889Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1917,856,05219,078,279
    nsv7063889RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1917,966,86119,189,088

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18758515inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18758515Submitted genomicNC_000019.10:g.178
    56052_19078279inv
    GRCh38 (hg38)NC_000019.10Chr1917,856,05219,078,279
    nssv18758515RemappedPerfectNC_000019.9:g.1796
    6861_19189088inv
    GRCh37.p13First PassNC_000019.9Chr1917,966,86119,189,088

    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)
    nssv187585154e-061276268
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