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nsv6640593

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,782

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 603 SVs from 40 studies. See in: genome view    
    Submitted genomic1,170,747-1,174,528Question Mark
    Overlapping variant regions from other studies: 603 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):1,106,127-1,109,908Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6640593Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr11,170,7471,174,528
    nsv6640593RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr11,106,1271,109,908

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18347214deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18347214Submitted genomicNC_000001.11:g.117
    0747_1174528del
    GRCh38 (hg38)NC_000001.11Chr11,170,7471,174,528
    nssv18347214RemappedPerfectNC_000001.10:g.110
    6127_1109908del
    GRCh37.p13First PassNC_000001.10Chr11,106,1271,109,908

    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)
    nssv183472144e-061276024
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