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nsv7070202

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,472,795

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 10450 SVs from 114 studies. See in: genome view    
    Submitted genomic27,330,033-30,802,827Question Mark
    Overlapping variant regions from other studies: 10450 SVs from 114 studies. See in: genome view    
    Remapped(Score: Perfect):27,618,962-31,091,756Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7070202Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1027,330,03330,802,827
    nsv7070202RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1027,618,96231,091,756

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18732228inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18732228Submitted genomicNC_000010.11:g.273
    30033_30802827inv
    GRCh38 (hg38)NC_000010.11Chr1027,330,03330,802,827
    nssv18732228RemappedPerfectNC_000010.10:g.276
    18962_31091756inv
    GRCh37.p13First PassNC_000010.10Chr1027,618,96231,091,756

    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)
    nssv187322284e-061276268
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