U.S. flag

An official website of the United States government

nsv7051473

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:531,786

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1359 SVs from 82 studies. See in: genome view    
    Submitted genomic45,349,403-45,881,188Question Mark
    Overlapping variant regions from other studies: 1359 SVs from 82 studies. See in: genome view    
    Remapped(Score: Perfect):45,349,505-45,881,290Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7051473Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr545,349,40345,881,188
    nsv7051473RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr545,349,50545,881,290

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18776284inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18776284Submitted genomicNC_000005.10:g.453
    49403_45881188inv
    GRCh38 (hg38)NC_000005.10Chr545,349,40345,881,188
    nssv18776284RemappedPerfectNC_000005.9:g.4534
    9505_45881290inv
    GRCh37.p13First PassNC_000005.9Chr545,349,50545,881,290

    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)
    nssv187762844e-061276268
    Support Center