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nsv6923239

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,079

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 144 SVs from 40 studies. See in: genome view    
    Submitted genomic127,939,626-127,943,704Question Mark
    Overlapping variant regions from other studies: 144 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):128,424,171-128,428,249Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6923239Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12127,939,626127,943,704
    nsv6923239RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12128,424,171128,428,249

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18358543deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18358543Submitted genomicNC_000012.12:g.127
    939626_127943704de
    l
    GRCh38 (hg38)NC_000012.12Chr12127,939,626127,943,704
    nssv18358543RemappedPerfectNC_000012.11:g.128
    424171_128428249de
    l
    GRCh37.p13First PassNC_000012.11Chr12128,424,171128,428,249

    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)
    nssv183585431.8e-055275560
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