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nsv6519065

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:231

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 136 SVs from 19 studies. See in: genome view    
    Submitted genomic75,965,355-75,965,585Question Mark
    Overlapping variant regions from other studies: 136 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):73,961,436-73,961,666Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6519065Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1775,965,35575,965,585
    nsv6519065RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1773,961,43673,961,666

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18038182deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18038182Submitted genomicNC_000017.11:g.759
    65355_75965585del
    GRCh38 (hg38)NC_000017.11Chr1775,965,35575,965,585
    nssv18038182RemappedPerfectNC_000017.10:g.739
    61436_73961666del
    GRCh37.p13First PassNC_000017.10Chr1773,961,43673,961,666

    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)
    nssv18038182<0.001132764
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