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nsv7072209

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:410,050

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2346 SVs from 94 studies. See in: genome view    
    Submitted genomic144,433,363-144,843,412Question Mark
    Overlapping variant regions from other studies: 2348 SVs from 94 studies. See in: genome view    
    Remapped(Score: Good):145,659,902-146,068,797Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7072209Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8144,433,363144,843,412
    nsv7072209RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8145,659,902146,068,797

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18783465inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18783465Submitted genomicNC_000008.11:g.144
    433363_144843412in
    v
    GRCh38 (hg38)NC_000008.11Chr8144,433,363144,843,412
    nssv18783465RemappedGoodNC_000008.10:g.145
    659902_146068797in
    v
    GRCh37.p13First PassNC_000008.10Chr8145,659,902146,068,797

    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)
    nssv187834652.9e-058268508
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