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nsv6670037

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:488,581

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1331 SVs from 89 studies. See in: genome view    
    Submitted genomic217,814,587-218,303,167Question Mark
    Overlapping variant regions from other studies: 1335 SVs from 89 studies. See in: genome view    
    Remapped(Score: Perfect):217,987,929-218,476,509Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6670037Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1217,814,587218,303,167
    nsv6670037RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1217,987,929218,476,509

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18608740duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18608740Submitted genomicNC_000001.11:g.217
    814587_218303167du
    p
    GRCh38 (hg38)NC_000001.11Chr1217,814,587218,303,167
    nssv18608740RemappedPerfectNC_000001.10:g.217
    987929_218476509du
    p
    GRCh37.p13First PassNC_000001.10Chr1217,987,929218,476,509

    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)
    nssv186087402.5e-057273978
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