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nsv7041986

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:417,745

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 781 SVs from 57 studies. See in: genome view    
    Submitted genomic148,256,171-148,673,915Question Mark
    Overlapping variant regions from other studies: 781 SVs from 57 studies. See in: genome view    
    Remapped(Score: Perfect):147,635,734-148,053,478Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7041986Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5148,256,171148,673,915
    nsv7041986RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5147,635,734148,053,478

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18774285inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18774285Submitted genomicNC_000005.10:g.148
    256171_148673915in
    v
    GRCh38 (hg38)NC_000005.10Chr5148,256,171148,673,915
    nssv18774285RemappedPerfectNC_000005.9:g.1476
    35734_148053478inv
    GRCh37.p13First PassNC_000005.9Chr5147,635,734148,053,478

    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)
    nssv187742854e-061276268
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