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nsv6514015

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16,282

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 165 SVs from 31 studies. See in: genome view    
    Submitted genomic40,682,883-40,699,164Question Mark
    Overlapping variant regions from other studies: 163 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):38,839,135-38,855,416Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6514015Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1740,682,88340,699,164
    nsv6514015RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1738,839,13538,855,416

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18184933duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18184933Submitted genomicNC_000017.11:g.406
    82883_40699164dup
    GRCh38 (hg38)NC_000017.11Chr1740,682,88340,699,164
    nssv18184933RemappedPerfectNC_000017.10:g.388
    39135_38855416dup
    GRCh37.p13First PassNC_000017.10Chr1738,839,13538,855,416

    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)
    nssv18184933<0.001139294
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