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nsv6931279

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,444

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 155 SVs from 39 studies. See in: genome view    
    Submitted genomic126,964,785-126,971,228Question Mark
    Overlapping variant regions from other studies: 155 SVs from 39 studies. See in: genome view    
    Remapped(Score: Good):127,449,331-127,455,773Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6931279Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12126,964,785126,971,228
    nsv6931279RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12127,449,331127,455,773

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18357308deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18357308Submitted genomicNC_000012.12:g.126
    964785_126971228de
    l
    GRCh38 (hg38)NC_000012.12Chr12126,964,785126,971,228
    nssv18357308RemappedGoodNC_000012.11:g.127
    449331_127455773de
    l
    GRCh37.p13First PassNC_000012.11Chr12127,449,331127,455,773

    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)
    nssv183573084e-061276212
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