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nsv7038478

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:249

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 116 SVs from 23 studies. See in: genome view    
    Submitted genomic124,844,312-124,844,560Question Mark
    Overlapping variant regions from other studies: 116 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):124,484,366-124,484,614Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7038478Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7124,844,312124,844,560
    nsv7038478RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7124,484,366124,484,614

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18778932inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18778932Submitted genomicNC_000007.14:g.124
    844312_124844560in
    v
    GRCh38 (hg38)NC_000007.14Chr7124,844,312124,844,560
    nssv18778932RemappedPerfectNC_000007.13:g.124
    484366_124484614in
    v
    GRCh37.p13First PassNC_000007.13Chr7124,484,366124,484,614

    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)
    nssv18778932<0.001242270886
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