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nsv6930867

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,638

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 145 SVs from 29 studies. See in: genome view    
    Submitted genomic29,275,067-29,285,704Question Mark
    Overlapping variant regions from other studies: 145 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):29,428,000-29,438,637Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6930867Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1229,275,06729,285,704
    nsv6930867RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1229,428,00029,438,637

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18360822deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18360822Submitted genomicNC_000012.12:g.292
    75067_29285704del
    GRCh38 (hg38)NC_000012.12Chr1229,275,06729,285,704
    nssv18360822RemappedPerfectNC_000012.11:g.294
    28000_29438637del
    GRCh37.p13First PassNC_000012.11Chr1229,428,00029,438,637

    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)
    nssv183608227e-062276262
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