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nsv7041748

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,707,826

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 10278 SVs from 120 studies. See in: genome view    
    Submitted genomic72,070,390-75,778,215Question Mark
    Overlapping variant regions from other studies: 10376 SVs from 120 studies. See in: genome view    
    Remapped(Score: Perfect):72,119,541-75,827,366Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7041748Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr372,070,39075,778,215
    nsv7041748RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr372,119,54175,827,366

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18772054inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18772054Submitted genomicNC_000003.12:g.720
    70390_75778215inv
    GRCh38 (hg38)NC_000003.12Chr372,070,39075,778,215
    nssv18772054RemappedPerfectNC_000003.11:g.721
    19541_75827366inv
    GRCh37.p13First PassNC_000003.11Chr372,119,54175,827,366

    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)
    nssv187720544e-061276268
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