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nsv6880533

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,547

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 146 SVs from 45 studies. See in: genome view    
    Submitted genomic52,764,459-52,774,005Question Mark
    Overlapping variant regions from other studies: 150 SVs from 45 studies. See in: genome view    
    Remapped(Score: Perfect):54,524,219-54,533,765Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6880533Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1052,764,45952,774,005
    nsv6880533RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1054,524,21954,533,765

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18337047deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18337047Submitted genomicNC_000010.11:g.527
    64459_52774005del
    GRCh38 (hg38)NC_000010.11Chr1052,764,45952,774,005
    nssv18337047RemappedPerfectNC_000010.10:g.545
    24219_54533765del
    GRCh37.p13First PassNC_000010.10Chr1054,524,21954,533,765

    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)
    nssv18337047<0.001203275804
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