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nsv7055264

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 122 SVs from 31 studies. See in: genome view    
    Submitted genomic141,397,100-141,397,151Question Mark
    Overlapping variant regions from other studies: 120 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):140,776,667-140,776,718Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7055264Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5141,397,100141,397,151
    nsv7055264RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5140,776,667140,776,718

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18774509inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18774509Submitted genomicNC_000005.10:g.141
    397100_141397151in
    v
    GRCh38 (hg38)NC_000005.10Chr5141,397,100141,397,151
    nssv18774509RemappedPerfectNC_000005.9:g.1407
    76667_140776718inv
    GRCh37.p13First PassNC_000005.9Chr5140,776,667140,776,718

    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)
    nssv18774509<0.00132273988
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