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nsv7053584

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,326,120

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 14504 SVs from 116 studies. See in: genome view    
    Submitted genomic144,534,922-150,861,041Question Mark
    Overlapping variant regions from other studies: 14504 SVs from 116 studies. See in: genome view    
    Remapped(Score: Perfect):143,914,485-150,240,603Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7053584Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5144,534,922150,861,041
    nsv7053584RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5143,914,485150,240,603

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18775138inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18775138Submitted genomicNC_000005.10:g.144
    534922_150861041in
    v
    GRCh38 (hg38)NC_000005.10Chr5144,534,922150,861,041
    nssv18775138RemappedPerfectNC_000005.9:g.1439
    14485_150240603inv
    GRCh37.p13First PassNC_000005.9Chr5143,914,485150,240,603

    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)
    nssv187751384e-061276268
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