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nsv7059677

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:688,594

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 5171 SVs from 114 studies. See in: genome view    
    Submitted genomic45,584,271-46,272,864Question Mark
    Overlapping variant regions from other studies: 4991 SVs from 114 studies. See in: genome view    
    Remapped(Score: Perfect):43,661,637-44,350,230Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7059677Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1745,584,27146,272,864
    nsv7059677RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1743,661,63744,350,230

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18758401inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18758401Submitted genomicNC_000017.11:g.455
    84271_46272864inv
    GRCh38 (hg38)NC_000017.11Chr1745,584,27146,272,864
    nssv18758401RemappedPerfectNC_000017.10:g.436
    61637_44350230inv
    GRCh37.p13First PassNC_000017.10Chr1743,661,63744,350,230

    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)
    nssv187584011.1e-053276256
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