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nsv6322033

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,290

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 119 SVs from 22 studies. See in: genome view    
    Submitted genomic207,806,429-207,812,718Question Mark
    Overlapping variant regions from other studies: 123 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):207,979,774-207,986,063Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6322033Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1207,806,429207,812,718
    nsv6322033RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1207,979,774207,986,063

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18057167deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18057167Submitted genomicNC_000001.11:g.207
    806429_207812718de
    l
    GRCh38 (hg38)NC_000001.11Chr1207,806,429207,812,718
    nssv18057167RemappedPerfectNC_000001.10:g.207
    979774_207986063de
    l
    GRCh37.p13First PassNC_000001.10Chr1207,979,774207,986,063

    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)
    nssv18057167<0.001239242
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