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nsv7017810

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:200,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1028 SVs from 74 studies. See in: genome view    
    Submitted genomic4,323,001-4,523,900Question Mark
    Overlapping variant regions from other studies: 1030 SVs from 74 studies. See in: genome view    
    Remapped(Score: Good):4,322,998-4,523,912Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7017810Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr194,323,0014,523,900
    nsv7017810RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr194,322,9984,523,912

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18638161duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18638161Submitted genomicNC_000019.10:g.432
    3001_4523900dup
    GRCh38 (hg38)NC_000019.10Chr194,323,0014,523,900
    nssv18638161RemappedGoodNC_000019.9:g.4322
    998_4523912dup
    GRCh37.p13First PassNC_000019.9Chr194,322,9984,523,912

    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)
    nssv186381614e-061274830
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