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nsv7039894

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,386

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 97 SVs from 34 studies. See in: genome view    
    Submitted genomic45,735,605-45,736,990Question Mark
    Overlapping variant regions from other studies: 97 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):45,775,204-45,776,589Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7039894Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr745,735,60545,736,990
    nsv7039894RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr745,775,20445,776,589

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18780222inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18780222Submitted genomicNC_000007.14:g.457
    35605_45736990inv
    GRCh38 (hg38)NC_000007.14Chr745,735,60545,736,990
    nssv18780222RemappedPerfectNC_000007.13:g.457
    75204_45776589inv
    GRCh37.p13First PassNC_000007.13Chr745,775,20445,776,589

    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)
    nssv187802222.5e-057275120
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