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nsv6885343

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,812

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 99 SVs from 23 studies. See in: genome view    
    Submitted genomic114,857,435-114,859,246Question Mark
    Overlapping variant regions from other studies: 99 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):116,617,194-116,619,005Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6885343Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10114,857,435114,859,246
    nsv6885343RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10116,617,194116,619,005

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18332040deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18332040Submitted genomicNC_000010.11:g.114
    857435_114859246de
    l
    GRCh38 (hg38)NC_000010.11Chr10114,857,435114,859,246
    nssv18332040RemappedPerfectNC_000010.10:g.116
    617194_116619005de
    l
    GRCh37.p13First PassNC_000010.10Chr10116,617,194116,619,005

    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)
    nssv183320404e-061275380
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