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nsv7070950

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:360,558

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1505 SVs from 92 studies. See in: genome view    
    Submitted genomic28,377,390-28,737,947Question Mark
    Overlapping variant regions from other studies: 1505 SVs from 92 studies. See in: genome view    
    Remapped(Score: Perfect):28,388,711-28,749,268Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7070950Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1628,377,39028,737,947
    nsv7070950RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1628,388,71128,749,268

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18757346inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18757346Submitted genomicNC_000016.10:g.283
    77390_28737947inv
    GRCh38 (hg38)NC_000016.10Chr1628,377,39028,737,947
    nssv18757346RemappedPerfectNC_000016.9:g.2838
    8711_28749268inv
    GRCh37.p13First PassNC_000016.9Chr1628,388,71128,749,268

    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)
    nssv187573460.0256286259664
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