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nsv7065384

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,857,491

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 7247 SVs from 105 studies. See in: genome view    
    Submitted genomic79,173,003-81,030,493Question Mark
    Overlapping variant regions from other studies: 7000 SVs from 105 studies. See in: genome view    
    Remapped(Score: Good):77,169,085-79,004,293Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7065384Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1779,173,00381,030,493
    nsv7065384RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1777,169,08579,004,293

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18757957inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18757957Submitted genomicNC_000017.11:g.791
    73003_81030493inv
    GRCh38 (hg38)NC_000017.11Chr1779,173,00381,030,493
    nssv18757957RemappedGoodNC_000017.10:g.771
    69085_79004293inv
    GRCh37.p13First PassNC_000017.10Chr1777,169,08579,004,293

    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)
    nssv187579572.2e-056270964
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