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nsv7057306

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:343,369

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1073 SVs from 77 studies. See in: genome view    
    Submitted genomic126,929,023-127,272,391Question Mark
    Overlapping variant regions from other studies: 1073 SVs from 77 studies. See in: genome view    
    Remapped(Score: Perfect):127,686,599-128,029,967Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7057306Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2126,929,023127,272,391
    nsv7057306RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2127,686,599128,029,967

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18765305inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18765305Submitted genomicNC_000002.12:g.126
    929023_127272391in
    v
    GRCh38 (hg38)NC_000002.12Chr2126,929,023127,272,391
    nssv18765305RemappedPerfectNC_000002.11:g.127
    686599_128029967in
    v
    GRCh37.p13First PassNC_000002.11Chr2127,686,599128,029,967

    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)
    nssv187653054e-061276268
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