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nsv6726155

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:619,942

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2901 SVs from 87 studies. See in: genome view    
    Submitted genomic39,630,360-40,250,301Question Mark
    Overlapping variant regions from other studies: 2901 SVs from 87 studies. See in: genome view    
    Remapped(Score: Perfect):39,631,980-40,251,921Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6726155Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr439,630,36040,250,301
    nsv6726155RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr439,631,98040,251,921

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18690955duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18690955Submitted genomicNC_000004.12:g.396
    30360_40250301dup
    GRCh38 (hg38)NC_000004.12Chr439,630,36040,250,301
    nssv18690955RemappedPerfectNC_000004.11:g.396
    31980_40251921dup
    GRCh37.p13First PassNC_000004.11Chr439,631,98040,251,921

    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)
    nssv186909554e-061270120
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