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nsv7046805

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:971

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 162 SVs from 22 studies. See in: genome view    
    Submitted genomic179,341,132-179,342,102Question Mark
    Overlapping variant regions from other studies: 164 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):179,310,267-179,311,237Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7046805Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1179,341,132179,342,102
    nsv7046805RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1179,310,267179,311,237

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18738373inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18738373Submitted genomicNC_000001.11:g.179
    341132_179342102in
    v
    GRCh38 (hg38)NC_000001.11Chr1179,341,132179,342,102
    nssv18738373RemappedPerfectNC_000001.10:g.179
    310267_179311237in
    v
    GRCh37.p13First PassNC_000001.10Chr1179,310,267179,311,237

    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)
    nssv187383734e-061276268
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