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nsv6334582

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:481

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 147 SVs from 31 studies. See in: genome view    
    Submitted genomic70,251,899-70,252,379Question Mark
    Overlapping variant regions from other studies: 147 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):70,717,582-70,718,062Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6334582Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr170,251,89970,252,379
    nsv6334582RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr170,717,58270,718,062

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18063589deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18063589Submitted genomicNC_000001.11:g.702
    51899_70252379del
    GRCh38 (hg38)NC_000001.11Chr170,251,89970,252,379
    nssv18063589RemappedPerfectNC_000001.10:g.707
    17582_70718062del
    GRCh37.p13First PassNC_000001.10Chr170,717,58270,718,062

    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)
    nssv180635890.0026738510
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