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nsv6950901

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:86,882

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 372 SVs from 51 studies. See in: genome view    
    Submitted genomic21,099,459-21,186,340Question Mark
    Overlapping variant regions from other studies: 372 SVs from 51 studies. See in: genome view    
    Remapped(Score: Perfect):21,567,618-21,654,499Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6950901Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1421,099,45921,186,340
    nsv6950901RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1421,567,61821,654,499

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18611054duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18611054Submitted genomicNC_000014.9:g.2109
    9459_21186340dup
    GRCh38 (hg38)NC_000014.9Chr1421,099,45921,186,340
    nssv18611054RemappedPerfectNC_000014.8:g.2156
    7618_21654499dup
    GRCh37.p13First PassNC_000014.8Chr1421,567,61821,654,499

    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)
    nssv186110544e-061263222
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