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nsv7043966

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:932,365

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2557 SVs from 87 studies. See in: genome view    
    Submitted genomic126,566,988-127,499,352Question Mark
    Overlapping variant regions from other studies: 2557 SVs from 87 studies. See in: genome view    
    Remapped(Score: Perfect):127,324,565-128,256,928Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7043966Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2126,566,988127,499,352
    nsv7043966RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2127,324,565128,256,928

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18765296inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18765296Submitted genomicNC_000002.12:g.126
    566988_127499352in
    v
    GRCh38 (hg38)NC_000002.12Chr2126,566,988127,499,352
    nssv18765296RemappedPerfectNC_000002.11:g.127
    324565_128256928in
    v
    GRCh37.p13First PassNC_000002.11Chr2127,324,565128,256,928

    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)
    nssv187652964e-061276268
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