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nsv7041311

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:26,935

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 172 SVs from 40 studies. See in: genome view    
    Submitted genomic71,317,709-71,344,643Question Mark
    Overlapping variant regions from other studies: 172 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):71,544,839-71,571,773Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7041311Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr271,317,70971,344,643
    nsv7041311RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr271,544,83971,571,773

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18769642inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18769642Submitted genomicNC_000002.12:g.713
    17709_71344643inv
    GRCh38 (hg38)NC_000002.12Chr271,317,70971,344,643
    nssv18769642RemappedPerfectNC_000002.11:g.715
    44839_71571773inv
    GRCh37.p13First PassNC_000002.11Chr271,544,83971,571,773

    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)
    nssv18769642<0.00191273978
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