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nsv6508491

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,491

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 151 SVs from 39 studies. See in: genome view    
    Submitted genomic67,895,696-67,906,186Question Mark
    Overlapping variant regions from other studies: 151 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):67,929,599-67,940,089Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6508491Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1667,895,69667,906,186
    nsv6508491RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1667,929,59967,940,089

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18030843deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18030843Submitted genomicNC_000016.10:g.678
    95696_67906186del
    GRCh38 (hg38)NC_000016.10Chr1667,895,69667,906,186
    nssv18030843RemappedPerfectNC_000016.9:g.6792
    9599_67940089del
    GRCh37.p13First PassNC_000016.9Chr1667,929,59967,940,089

    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)
    nssv18030843<0.001138790
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