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nsv7058857

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:202,238

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 465 SVs from 63 studies. See in: genome view    
    Submitted genomic122,808,418-123,010,655Question Mark
    Overlapping variant regions from other studies: 465 SVs from 63 studies. See in: genome view    
    Remapped(Score: Perfect):124,567,934-124,770,171Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7058857Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10122,808,418123,010,655
    nsv7058857RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10124,567,934124,770,171

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18740297inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18740297Submitted genomicNC_000010.11:g.122
    808418_123010655in
    v
    GRCh38 (hg38)NC_000010.11Chr10122,808,418123,010,655
    nssv18740297RemappedPerfectNC_000010.10:g.124
    567934_124770171in
    v
    GRCh37.p13First PassNC_000010.10Chr10124,567,934124,770,171

    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)
    nssv187402974e-061276268
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