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nsv7077051

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,608,681

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 7181 SVs from 100 studies. See in: genome view    
    Submitted genomic63,334,072-65,942,752Question Mark
    Overlapping variant regions from other studies: 7181 SVs from 100 studies. See in: genome view    
    Remapped(Score: Perfect):63,800,790-66,409,470Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7077051Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1463,334,07265,942,752
    nsv7077051RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1463,800,79066,409,470

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18753913inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18753913Submitted genomicNC_000014.9:g.6333
    4072_65942752inv
    GRCh38 (hg38)NC_000014.9Chr1463,334,07265,942,752
    nssv18753913RemappedPerfectNC_000014.8:g.6380
    0790_66409470inv
    GRCh37.p13First PassNC_000014.8Chr1463,800,79066,409,470

    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)
    nssv187539134.6e-0512274402
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