U.S. flag

An official website of the United States government

nsv7051439

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:281,065

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1197 SVs from 77 studies. See in: genome view    
    Submitted genomic245,486,831-245,767,895Question Mark
    Overlapping variant regions from other studies: 1200 SVs from 77 studies. See in: genome view    
    Remapped(Score: Perfect):245,650,133-245,931,197Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7051439Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1245,486,831245,767,895
    nsv7051439RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1245,650,133245,931,197

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18759467inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18759467Submitted genomicNC_000001.11:g.245
    486831_245767895in
    v
    GRCh38 (hg38)NC_000001.11Chr1245,486,831245,767,895
    nssv18759467RemappedPerfectNC_000001.10:g.245
    650133_245931197in
    v
    GRCh37.p13First PassNC_000001.10Chr1245,650,133245,931,197

    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)
    nssv187594674e-061276268
    Support Center