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nsv6893893

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,997

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 125 SVs from 31 studies. See in: genome view    
    Submitted genomic50,447,214-50,454,210Question Mark
    Overlapping variant regions from other studies: 142 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):52,206,974-52,213,970Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6893893Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1050,447,21450,454,210
    nsv6893893RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1052,206,97452,213,970

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18336844deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18336844Submitted genomicNC_000010.11:g.504
    47214_50454210del
    GRCh38 (hg38)NC_000010.11Chr1050,447,21450,454,210
    nssv18336844RemappedPerfectNC_000010.10:g.522
    06974_52213970del
    GRCh37.p13First PassNC_000010.10Chr1052,206,97452,213,970

    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)
    nssv183368441.1e-053275760
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