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nsv6324116

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:415

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 122 SVs from 20 studies. See in: genome view    
    Submitted genomic53,928,942-53,929,356Question Mark
    Overlapping variant regions from other studies: 122 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):54,394,615-54,395,029Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6324116Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr153,928,94253,929,356
    nsv6324116RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr154,394,61554,395,029

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18061528deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18061528Submitted genomicNC_000001.11:g.539
    28942_53929356del
    GRCh38 (hg38)NC_000001.11Chr153,928,94253,929,356
    nssv18061528RemappedPerfectNC_000001.10:g.543
    94615_54395029del
    GRCh37.p13First PassNC_000001.10Chr154,394,61554,395,029

    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)
    nssv18061528<0.0013337432
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