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nsv6934787

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:175

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 95 SVs from 31 studies. See in: genome view    
    Submitted genomic95,158,574-95,158,748Question Mark
    Overlapping variant regions from other studies: 95 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):95,552,350-95,552,524Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6934787Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1295,158,57495,158,748
    nsv6934787RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1295,552,35095,552,524

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18600368duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18600368Submitted genomicNC_000012.12:g.951
    58574_95158748dup
    GRCh38 (hg38)NC_000012.12Chr1295,158,57495,158,748
    nssv18600368RemappedPerfectNC_000012.11:g.955
    52350_95552524dup
    GRCh37.p13First PassNC_000012.11Chr1295,552,35095,552,524

    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)
    nssv186003688e-0519231468
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