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nsv7073131

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,839

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 126 SVs from 24 studies. See in: genome view    
    Submitted genomic36,200,306-36,203,144Question Mark
    Overlapping variant regions from other studies: 126 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):36,691,208-36,694,046Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7073131Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1936,200,30636,203,144
    nsv7073131RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1936,691,20836,694,046

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18758589inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18758589Submitted genomicNC_000019.10:g.362
    00306_36203144inv
    GRCh38 (hg38)NC_000019.10Chr1936,200,30636,203,144
    nssv18758589RemappedPerfectNC_000019.9:g.3669
    1208_36694046inv
    GRCh37.p13First PassNC_000019.9Chr1936,691,20836,694,046

    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)
    nssv18758589<0.00143267956
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