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nsv6496579

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:616

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 115 SVs from 16 studies. See in: genome view    
    Submitted genomic40,040,178-40,040,793Question Mark
    Overlapping variant regions from other studies: 113 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):38,196,431-38,197,046Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6496579Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1740,040,17840,040,793
    nsv6496579RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1738,196,43138,197,046

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18188310duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18188310Submitted genomicNC_000017.11:g.400
    40178_40040793dup
    GRCh38 (hg38)NC_000017.11Chr1740,040,17840,040,793
    nssv18188310RemappedPerfectNC_000017.10:g.381
    96431_38197046dup
    GRCh37.p13First PassNC_000017.10Chr1738,196,43138,197,046

    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)
    nssv18188310<0.001138420
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