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nsv6466690

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:832

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 97 SVs from 19 studies. See in: genome view    
    Submitted genomic111,525,636-111,526,467Question Mark
    Overlapping variant regions from other studies: 97 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):111,396,361-111,397,192Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6466690Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11111,525,636111,526,467
    nsv6466690RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11111,396,361111,397,192

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17986767deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17986767Submitted genomicNC_000011.10:g.111
    525636_111526467de
    l
    GRCh38 (hg38)NC_000011.10Chr11111,525,636111,526,467
    nssv17986767RemappedPerfectNC_000011.9:g.1113
    96361_111397192del
    GRCh37.p13First PassNC_000011.9Chr11111,396,361111,397,192

    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)
    nssv17986767<0.001136818
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