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nsv6966826

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:215,439

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 853 SVs from 69 studies. See in: genome view    
    Submitted genomic10,646,382-10,861,820Question Mark
    Overlapping variant regions from other studies: 853 SVs from 69 studies. See in: genome view    
    Remapped(Score: Perfect):10,740,239-10,955,677Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6966826Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1610,646,38210,861,820
    nsv6966826RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1610,740,23910,955,677

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18620497duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18620497Submitted genomicNC_000016.10:g.106
    46382_10861820dup
    GRCh38 (hg38)NC_000016.10Chr1610,646,38210,861,820
    nssv18620497RemappedPerfectNC_000016.9:g.1074
    0239_10955677dup
    GRCh37.p13First PassNC_000016.9Chr1610,740,23910,955,677

    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)
    nssv186204974e-061275580
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