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nsv6440768

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:376,005

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1272 SVs from 76 studies. See in: genome view    
    Submitted genomic53,417,465-53,793,469Question Mark
    Overlapping variant regions from other studies: 1276 SVs from 76 studies. See in: genome view    
    Remapped(Score: Perfect):55,177,225-55,553,229Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6440768Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1053,417,46553,793,469
    nsv6440768RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1055,177,22555,553,229

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17981782deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17981782Submitted genomicNC_000010.11:g.534
    17465_53793469del
    GRCh38 (hg38)NC_000010.11Chr1053,417,46553,793,469
    nssv17981782RemappedPerfectNC_000010.10:g.551
    77225_55553229del
    GRCh37.p13First PassNC_000010.10Chr1055,177,22555,553,229

    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)
    nssv17981782<0.001139094
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