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nsv7057345

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:828,124

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2736 SVs from 97 studies. See in: genome view    
    Submitted genomic129,898,796-130,726,919Question Mark
    Overlapping variant regions from other studies: 2736 SVs from 97 studies. See in: genome view    
    Remapped(Score: Perfect):130,656,369-131,484,492Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7057345Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2129,898,796130,726,919
    nsv7057345RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2130,656,369131,484,492

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18765346inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18765346Submitted genomicNC_000002.12:g.129
    898796_130726919in
    v
    GRCh38 (hg38)NC_000002.12Chr2129,898,796130,726,919
    nssv18765346RemappedPerfectNC_000002.11:g.130
    656369_131484492in
    v
    GRCh37.p13First PassNC_000002.11Chr2130,656,369131,484,492

    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)
    nssv187653464e-061276268
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