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nsv6971934

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:207

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 77 SVs from 17 studies. See in: genome view    
    Submitted genomic64,969,354-64,969,560Question Mark
    Overlapping variant regions from other studies: 77 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):65,436,072-65,436,278Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6971934Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1464,969,35464,969,560
    nsv6971934RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1465,436,07265,436,278

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18614593duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18614593Submitted genomicNC_000014.9:g.6496
    9354_64969560dup
    GRCh38 (hg38)NC_000014.9Chr1464,969,35464,969,560
    nssv18614593RemappedPerfectNC_000014.8:g.6543
    6072_65436278dup
    GRCh37.p13First PassNC_000014.8Chr1465,436,07265,436,278

    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)
    nssv186145934e-061236100
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