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nsv7014855

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:71,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 429 SVs from 57 studies. See in: genome view    
    Submitted genomic55,312,701-55,384,200Question Mark
    Overlapping variant regions from other studies: 429 SVs from 57 studies. See in: genome view    
    Remapped(Score: Perfect):55,824,069-55,895,568Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7014855Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1955,312,70155,384,200
    nsv7014855RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1955,824,06955,895,568

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18638963duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18638963Submitted genomicNC_000019.10:g.553
    12701_55384200dup
    GRCh38 (hg38)NC_000019.10Chr1955,312,70155,384,200
    nssv18638963RemappedPerfectNC_000019.9:g.5582
    4069_55895568dup
    GRCh37.p13First PassNC_000019.9Chr1955,824,06955,895,568

    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)
    nssv186389638e-062242880
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