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nsv7063173

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:204,995

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 684 SVs from 72 studies. See in: genome view    
    Submitted genomic59,885,051-60,090,045Question Mark
    Overlapping variant regions from other studies: 684 SVs from 72 studies. See in: genome view    
    Remapped(Score: Perfect):57,962,412-58,167,406Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7063173Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1759,885,05160,090,045
    nsv7063173RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1757,962,41258,167,406

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18758458inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18758458Submitted genomicNC_000017.11:g.598
    85051_60090045inv
    GRCh38 (hg38)NC_000017.11Chr1759,885,05160,090,045
    nssv18758458RemappedPerfectNC_000017.10:g.579
    62412_58167406inv
    GRCh37.p13First PassNC_000017.10Chr1757,962,41258,167,406

    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)
    nssv187584584e-061276268
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