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nsv6667308

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 128 SVs from 22 studies. See in: genome view    
    Submitted genomic231,377,901-231,384,000Question Mark
    Overlapping variant regions from other studies: 131 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):231,513,647-231,519,746Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6667308Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1231,377,901231,384,000
    nsv6667308RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1231,513,647231,519,746

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18609217duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18609217Submitted genomicNC_000001.11:g.231
    377901_231384000du
    p
    GRCh38 (hg38)NC_000001.11Chr1231,377,901231,384,000
    nssv18609217RemappedPerfectNC_000001.10:g.231
    513647_231519746du
    p
    GRCh37.p13First PassNC_000001.10Chr1231,513,647231,519,746

    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)
    nssv186092174e-061275170
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