U.S. flag

An official website of the United States government

nsv7060070

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:102,517

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 406 SVs from 48 studies. See in: genome view    
    Submitted genomic67,336,782-67,439,298Question Mark
    Overlapping variant regions from other studies: 406 SVs from 48 studies. See in: genome view    
    Remapped(Score: Perfect):65,332,898-65,435,414Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7060070Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1767,336,78267,439,298
    nsv7060070RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1765,332,89865,435,414

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18758995inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18758995Submitted genomicNC_000017.11:g.673
    36782_67439298inv
    GRCh38 (hg38)NC_000017.11Chr1767,336,78267,439,298
    nssv18758995RemappedPerfectNC_000017.10:g.653
    32898_65435414inv
    GRCh37.p13First PassNC_000017.10Chr1765,332,89865,435,414

    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)
    nssv187589951.1e-053276226
    Support Center