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nsv7067191

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:417,410

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1323 SVs from 84 studies. See in: genome view    
    Submitted genomic52,189,676-52,607,085Question Mark
    Overlapping variant regions from other studies: 1323 SVs from 84 studies. See in: genome view    
    Remapped(Score: Perfect):52,763,811-53,181,220Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7067191Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1352,189,67652,607,085
    nsv7067191RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1352,763,81153,181,220

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18752995inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18752995Submitted genomicNC_000013.11:g.521
    89676_52607085inv
    GRCh38 (hg38)NC_000013.11Chr1352,189,67652,607,085
    nssv18752995RemappedPerfectNC_000013.10:g.527
    63811_53181220inv
    GRCh37.p13First PassNC_000013.10Chr1352,763,81153,181,220

    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)
    nssv187529957e-062274744
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