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nsv6933471

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,102

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 122 SVs from 29 studies. See in: genome view    
    Submitted genomic125,045,505-125,047,606Question Mark
    Overlapping variant regions from other studies: 122 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):125,530,051-125,532,152Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6933471Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12125,045,505125,047,606
    nsv6933471RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12125,530,051125,532,152

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18593968duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18593968Submitted genomicNC_000012.12:g.125
    045505_125047606du
    p
    GRCh38 (hg38)NC_000012.12Chr12125,045,505125,047,606
    nssv18593968RemappedPerfectNC_000012.11:g.125
    530051_125532152du
    p
    GRCh37.p13First PassNC_000012.11Chr12125,530,051125,532,152

    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)
    nssv185939687e-062265168
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