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nsv7057394

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:114,875

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 976 SVs from 79 studies. See in: genome view    
    Submitted genomic247,044,533-247,159,407Question Mark
    Overlapping variant regions from other studies: 979 SVs from 79 studies. See in: genome view    
    Remapped(Score: Perfect):247,207,835-247,322,709Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7057394Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1247,044,533247,159,407
    nsv7057394RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1247,207,835247,322,709

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18759494inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18759494Submitted genomicNC_000001.11:g.247
    044533_247159407in
    v
    GRCh38 (hg38)NC_000001.11Chr1247,044,533247,159,407
    nssv18759494RemappedPerfectNC_000001.10:g.247
    207835_247322709in
    v
    GRCh37.p13First PassNC_000001.10Chr1247,207,835247,322,709

    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)
    nssv187594944e-061276268
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