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nsv7067530

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:682,495

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2113 SVs from 101 studies. See in: genome view    
    Submitted genomic79,527,707-80,210,201Question Mark
    Overlapping variant regions from other studies: 2184 SVs from 105 studies. See in: genome view    
    Remapped(Score: Perfect):81,287,463-81,969,957Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7067530Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1079,527,70780,210,201
    nsv7067530RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1081,287,46381,969,957

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18745843inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18745843Submitted genomicNC_000010.11:g.795
    27707_80210201inv
    GRCh38 (hg38)NC_000010.11Chr1079,527,70780,210,201
    nssv18745843RemappedPerfectNC_000010.10:g.812
    87463_81969957inv
    GRCh37.p13First PassNC_000010.10Chr1081,287,46381,969,957

    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)
    nssv187458434e-061276268
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