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nsv7072185

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:309,601

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1122 SVs from 84 studies. See in: genome view    
    Submitted genomic52,248,474-52,558,074Question Mark
    Overlapping variant regions from other studies: 1122 SVs from 84 studies. See in: genome view    
    Remapped(Score: Perfect):52,822,609-53,132,209Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7072185Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1352,248,47452,558,074
    nsv7072185RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1352,822,60953,132,209

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18753004inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18753004Submitted genomicNC_000013.11:g.522
    48474_52558074inv
    GRCh38 (hg38)NC_000013.11Chr1352,248,47452,558,074
    nssv18753004RemappedPerfectNC_000013.10:g.528
    22609_53132209inv
    GRCh37.p13First PassNC_000013.10Chr1352,822,60953,132,209

    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)
    nssv187530044e-061276268
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