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nsv6680629

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:26,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 362 SVs from 64 studies. See in: genome view    
    Submitted genomic208,167,201-208,194,000Question Mark
    Overlapping variant regions from other studies: 362 SVs from 64 studies. See in: genome view    
    Remapped(Score: Perfect):209,031,925-209,058,724Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6680629Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2208,167,201208,194,000
    nsv6680629RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2209,031,925209,058,724

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18448379deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18448379Submitted genomicNC_000002.12:g.208
    167201_208194000de
    l
    GRCh38 (hg38)NC_000002.12Chr2208,167,201208,194,000
    nssv18448379RemappedPerfectNC_000002.11:g.209
    031925_209058724de
    l
    GRCh37.p13First PassNC_000002.11Chr2209,031,925209,058,724

    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)
    nssv18448379<0.001139253670
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