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nsv7008196

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:59

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 318 SVs from 22 studies. See in: genome view    
    Submitted genomic72,635,151-72,635,209Question Mark
    Overlapping variant regions from other studies: 318 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):70,302,386-70,302,444Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7008196Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1872,635,15172,635,209
    nsv7008196RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1870,302,38670,302,444

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18637595duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18637595Submitted genomicNC_000018.10:g.726
    35151_72635209dup
    GRCh38 (hg38)NC_000018.10Chr1872,635,15172,635,209
    nssv18637595RemappedPerfectNC_000018.9:g.7030
    2386_70302444dup
    GRCh37.p13First PassNC_000018.9Chr1870,302,38670,302,444

    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)
    nssv186375955e-061213360
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