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nsv7039912

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 259 SVs from 29 studies. See in: genome view    
    Submitted genomic245,298,221-245,305,020Question Mark
    Overlapping variant regions from other studies: 262 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):245,461,523-245,468,322Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7039912Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1245,298,221245,305,020
    nsv7039912RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1245,461,523245,468,322

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18759463inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18759463Submitted genomicNC_000001.11:g.245
    298221_245305020in
    v
    GRCh38 (hg38)NC_000001.11Chr1245,298,221245,305,020
    nssv18759463RemappedPerfectNC_000001.10:g.245
    461523_245468322in
    v
    GRCh37.p13First PassNC_000001.10Chr1245,461,523245,468,322

    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)
    nssv187594634e-061276268
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