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nsv7073451

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,830,453

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 23855 SVs from 123 studies. See in: genome view    
    Submitted genomic39,843,646-49,674,098Question Mark
    Overlapping variant regions from other studies: 23856 SVs from 123 studies. See in: genome view    
    Remapped(Score: Perfect):40,417,783-50,248,234Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7073451Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1339,843,64649,674,098
    nsv7073451RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1340,417,78350,248,234

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18753595inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18753595Submitted genomicNC_000013.11:g.398
    43646_49674098inv
    GRCh38 (hg38)NC_000013.11Chr1339,843,64649,674,098
    nssv18753595RemappedPerfectNC_000013.10:g.404
    17783_50248234inv
    GRCh37.p13First PassNC_000013.10Chr1340,417,78350,248,234

    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)
    nssv187535954e-061276268
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