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nsv6789367

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,233,132

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2832 SVs from 96 studies. See in: genome view    
    Submitted genomic48,645,525-49,878,656Question Mark
    Overlapping variant regions from other studies: 2818 SVs from 96 studies. See in: genome view    
    Remapped(Score: Good):48,613,261-49,846,369Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6789367Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr648,645,52549,878,656
    nsv6789367RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr648,613,26149,846,369

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18715831duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18715831Submitted genomicNC_000006.12:g.486
    45525_49878656dup
    GRCh38 (hg38)NC_000006.12Chr648,645,52549,878,656
    nssv18715831RemappedGoodNC_000006.11:g.486
    13261_49846369dup
    GRCh37.p13First PassNC_000006.11Chr648,613,26149,846,369

    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)
    nssv187158314e-061270702
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