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nsv6747056

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,713

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 156 SVs from 29 studies. See in: genome view    
    Submitted genomic87,482,560-87,490,272Question Mark
    Overlapping variant regions from other studies: 156 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):88,403,712-88,411,424Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6747056Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr487,482,56087,490,272
    nsv6747056RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr488,403,71288,411,424

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18501688deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18501688Submitted genomicNC_000004.12:g.874
    82560_87490272del
    GRCh38 (hg38)NC_000004.12Chr487,482,56087,490,272
    nssv18501688RemappedPerfectNC_000004.11:g.884
    03712_88411424del
    GRCh37.p13First PassNC_000004.11Chr488,403,71288,411,424

    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)
    nssv185016882.1e-056275474
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