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nsv6887736

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,203

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 115 SVs from 29 studies. See in: genome view    
    Submitted genomic73,803,840-73,817,042Question Mark
    Overlapping variant regions from other studies: 115 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):75,563,598-75,576,800Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6887736Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1073,803,84073,817,042
    nsv6887736RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1075,563,59875,576,800

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18578355duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18578355Submitted genomicNC_000010.11:g.738
    03840_73817042dup
    GRCh38 (hg38)NC_000010.11Chr1073,803,84073,817,042
    nssv18578355RemappedPerfectNC_000010.10:g.755
    63598_75576800dup
    GRCh37.p13First PassNC_000010.10Chr1075,563,59875,576,800

    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)
    nssv185783554e-061275638
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