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nsv6492096

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 79 SVs from 22 studies. See in: genome view    
    Submitted genomic70,641,501-70,643,800Question Mark
    Overlapping variant regions from other studies: 79 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):71,108,218-71,110,517Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6492096Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1470,641,50170,643,800
    nsv6492096RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1471,108,21871,110,517

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18184846duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18184846Submitted genomicNC_000014.9:g.7064
    1501_70643800dup
    GRCh38 (hg38)NC_000014.9Chr1470,641,50170,643,800
    nssv18184846RemappedPerfectNC_000014.8:g.7110
    8218_71110517dup
    GRCh37.p13First PassNC_000014.8Chr1471,108,21871,110,517

    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)
    nssv18184846<0.001237082
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