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nsv6921687

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,480

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 147 SVs from 28 studies. See in: genome view    
    Submitted genomic29,276,762-29,286,241Question Mark
    Overlapping variant regions from other studies: 147 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):29,429,695-29,439,174Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6921687Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1229,276,76229,286,241
    nsv6921687RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1229,429,69529,439,174

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18360823deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18360823Submitted genomicNC_000012.12:g.292
    76762_29286241del
    GRCh38 (hg38)NC_000012.12Chr1229,276,76229,286,241
    nssv18360823RemappedPerfectNC_000012.11:g.294
    29695_29439174del
    GRCh37.p13First PassNC_000012.11Chr1229,429,69529,439,174

    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)
    nssv183608234e-061276250
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