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nsv7041668

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16,298

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 225 SVs from 38 studies. See in: genome view    
    Submitted genomic202,389,716-202,406,013Question Mark
    Overlapping variant regions from other studies: 225 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):203,254,439-203,270,736Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7041668Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2202,389,716202,406,013
    nsv7041668RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2203,254,439203,270,736

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18766756inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18766756Submitted genomicNC_000002.12:g.202
    389716_202406013in
    v
    GRCh38 (hg38)NC_000002.12Chr2202,389,716202,406,013
    nssv18766756RemappedPerfectNC_000002.11:g.203
    254439_203270736in
    v
    GRCh37.p13First PassNC_000002.11Chr2203,254,439203,270,736

    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)
    nssv187667564e-061276268
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