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nsv7048610

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,716,762

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4817 SVs from 112 studies. See in: genome view    
    Submitted genomic129,502,833-131,219,594Question Mark
    Overlapping variant regions from other studies: 4817 SVs from 112 studies. See in: genome view    
    Remapped(Score: Perfect):130,260,406-131,977,167Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7048610Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2129,502,833131,219,594
    nsv7048610RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2130,260,406131,977,167

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18765339inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18765339Submitted genomicNC_000002.12:g.129
    502833_131219594in
    v
    GRCh38 (hg38)NC_000002.12Chr2129,502,833131,219,594
    nssv18765339RemappedPerfectNC_000002.11:g.130
    260406_131977167in
    v
    GRCh37.p13First PassNC_000002.11Chr2130,260,406131,977,167

    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)
    nssv187653394e-061276266
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