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nsv6929121

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,132

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 149 SVs from 27 studies. See in: genome view    
    Submitted genomic29,284,557-29,295,688Question Mark
    Overlapping variant regions from other studies: 149 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):29,437,490-29,448,621Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6929121Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1229,284,55729,295,688
    nsv6929121RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1229,437,49029,448,621

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18360824deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18360824Submitted genomicNC_000012.12:g.292
    84557_29295688del
    GRCh38 (hg38)NC_000012.12Chr1229,284,55729,295,688
    nssv18360824RemappedPerfectNC_000012.11:g.294
    37490_29448621del
    GRCh37.p13First PassNC_000012.11Chr1229,437,49029,448,621

    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)
    nssv183608247e-062276252
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