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nsv6675353

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:56

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 85 SVs from 18 studies. See in: genome view    
    Submitted genomic9,884,836-9,884,891Question Mark
    Overlapping variant regions from other studies: 85 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):10,024,965-10,025,020Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6675353Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr29,884,8369,884,891
    nsv6675353RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr210,024,96510,025,020

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18470834deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18470834Submitted genomicNC_000002.12:g.988
    4836_9884891del
    GRCh38 (hg38)NC_000002.12Chr29,884,8369,884,891
    nssv18470834RemappedPerfectNC_000002.11:g.100
    24965_10025020del
    GRCh37.p13First PassNC_000002.11Chr210,024,96510,025,020

    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)
    nssv18470834<0.001106241846
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