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nsv6884552

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:172,932

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 650 SVs from 66 studies. See in: genome view    
    Submitted genomic6,629,858-6,802,789Question Mark
    Overlapping variant regions from other studies: 650 SVs from 66 studies. See in: genome view    
    Remapped(Score: Perfect):6,671,820-6,844,751Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6884552Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr106,629,8586,802,789
    nsv6884552RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr106,671,8206,844,751

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18338400deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18338400Submitted genomicNC_000010.11:g.662
    9858_6802789del
    GRCh38 (hg38)NC_000010.11Chr106,629,8586,802,789
    nssv18338400RemappedPerfectNC_000010.10:g.667
    1820_6844751del
    GRCh37.p13First PassNC_000010.10Chr106,671,8206,844,751

    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)
    nssv18338400<0.00126252496
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