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nsv6318273

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,891

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 169 SVs from 34 studies. See in: genome view    
    Submitted genomic226,070,498-226,077,388Question Mark
    Overlapping variant regions from other studies: 172 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):226,258,199-226,265,089Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6318273Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1226,070,498226,077,388
    nsv6318273RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1226,258,199226,265,089

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18202703duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18202703Submitted genomicNC_000001.11:g.226
    070498_226077388du
    p
    GRCh38 (hg38)NC_000001.11Chr1226,070,498226,077,388
    nssv18202703RemappedPerfectNC_000001.10:g.226
    258199_226265089du
    p
    GRCh37.p13First PassNC_000001.10Chr1226,258,199226,265,089

    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)
    nssv182027030.0026339254
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