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nsv6664015

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,156

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 133 SVs from 17 studies. See in: genome view    
    Submitted genomic36,854,429-36,855,584Question Mark
    Overlapping variant regions from other studies: 133 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):37,081,572-37,082,727Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6664015Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr236,854,42936,855,584
    nsv6664015RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr237,081,57237,082,727

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18663320duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18663320Submitted genomicNC_000002.12:g.368
    54429_36855584dup
    GRCh38 (hg38)NC_000002.12Chr236,854,42936,855,584
    nssv18663320RemappedPerfectNC_000002.11:g.370
    81572_37082727dup
    GRCh37.p13First PassNC_000002.11Chr237,081,57237,082,727

    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)
    nssv186633204e-061264366
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