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nsv7038295

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:40

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 240 SVs from 20 studies. See in: genome view    
    Submitted genomic245,404,992-245,405,031Question Mark
    Overlapping variant regions from other studies: 243 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):245,568,294-245,568,333Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7038295Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1245,404,992245,405,031
    nsv7038295RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1245,568,294245,568,333

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18759466inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18759466Submitted genomicNC_000001.11:g.245
    404992_245405031in
    v
    GRCh38 (hg38)NC_000001.11Chr1245,404,992245,405,031
    nssv18759466RemappedPerfectNC_000001.10:g.245
    568294_245568333in
    v
    GRCh37.p13First PassNC_000001.10Chr1245,568,294245,568,333

    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)
    nssv187594664e-061276268
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