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nsv6905451

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:65,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 300 SVs from 63 studies. See in: genome view    
    Submitted genomic5,091,001-5,156,700Question Mark
    Overlapping variant regions from other studies: 300 SVs from 63 studies. See in: genome view    
    Remapped(Score: Perfect):5,112,231-5,177,930Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6905451Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr115,091,0015,156,700
    nsv6905451RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr115,112,2315,177,930

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18351418deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18351418Submitted genomicNC_000011.10:g.509
    1001_5156700del
    GRCh38 (hg38)NC_000011.10Chr115,091,0015,156,700
    nssv18351418RemappedPerfectNC_000011.9:g.5112
    231_5177930del
    GRCh37.p13First PassNC_000011.9Chr115,112,2315,177,930

    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)
    nssv183514181.4e-054275386
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