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nsv7050683

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:53

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 133 SVs from 26 studies. See in: genome view    
    Submitted genomic157,327,051-157,327,103Question Mark
    Overlapping variant regions from other studies: 133 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):158,183,563-158,183,615Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7050683Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2157,327,051157,327,103
    nsv7050683RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2158,183,563158,183,615

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18766054inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18766054Submitted genomicNC_000002.12:g.157
    327051_157327103in
    v
    GRCh38 (hg38)NC_000002.12Chr2157,327,051157,327,103
    nssv18766054RemappedPerfectNC_000002.11:g.158
    183563_158183615in
    v
    GRCh37.p13First PassNC_000002.11Chr2158,183,563158,183,615

    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)
    nssv187660540.001283274600
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