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nsv6766352

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,307,640

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 18445 SVs from 115 studies. See in: genome view    
    Submitted genomic52,086,933-59,394,572Question Mark
    Overlapping variant regions from other studies: 18445 SVs from 115 studies. See in: genome view    
    Remapped(Score: Perfect):51,382,767-58,690,398Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6766352Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr552,086,93359,394,572
    nsv6766352RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr551,382,76758,690,398

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18513647deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18513647Submitted genomicNC_000005.10:g.520
    86933_59394572del
    GRCh38 (hg38)NC_000005.10Chr552,086,93359,394,572
    nssv18513647RemappedPerfectNC_000005.9:g.5138
    2767_58690398del
    GRCh37.p13First PassNC_000005.9Chr551,382,76758,690,398

    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)
    nssv185136474e-061253844
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