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nsv7055170

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,648

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 89 SVs from 22 studies. See in: genome view    
    Submitted genomic147,041,150-147,046,797Question Mark
    Overlapping variant regions from other studies: 89 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):146,420,713-146,426,360Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7055170Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5147,041,150147,046,797
    nsv7055170RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5146,420,713146,426,360

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18775186inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18775186Submitted genomicNC_000005.10:g.147
    041150_147046797in
    v
    GRCh38 (hg38)NC_000005.10Chr5147,041,150147,046,797
    nssv18775186RemappedPerfectNC_000005.9:g.1464
    20713_146426360inv
    GRCh37.p13First PassNC_000005.9Chr5146,420,713146,426,360

    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)
    nssv187751861.1e-053275088
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