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nsv6877415

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:796,615

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2919 SVs from 92 studies. See in: genome view    
    Submitted genomic18,863,175-19,659,789Question Mark
    Overlapping variant regions from other studies: 2925 SVs from 92 studies. See in: genome view    
    Remapped(Score: Perfect):18,863,173-19,659,787Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6877415Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr918,863,17519,659,789
    nsv6877415RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr918,863,17319,659,787

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18745559duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18745559Submitted genomicNC_000009.12:g.188
    63175_19659789dup
    GRCh38 (hg38)NC_000009.12Chr918,863,17519,659,789
    nssv18745559RemappedPerfectNC_000009.11:g.188
    63173_19659787dup
    GRCh37.p13First PassNC_000009.11Chr918,863,17319,659,787

    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)
    nssv187455594e-061272580
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