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nsv6814660

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:129,008

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 652 SVs from 74 studies. See in: genome view    
    Submitted genomic17,386,479-17,515,486Question Mark
    Overlapping variant regions from other studies: 652 SVs from 74 studies. See in: genome view    
    Remapped(Score: Perfect):17,426,103-17,555,110Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6814660Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr717,386,47917,515,486
    nsv6814660RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr717,426,10317,555,110

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18724180duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18724180Submitted genomicNC_000007.14:g.173
    86479_17515486dup
    GRCh38 (hg38)NC_000007.14Chr717,386,47917,515,486
    nssv18724180RemappedPerfectNC_000007.13:g.174
    26103_17555110dup
    GRCh37.p13First PassNC_000007.13Chr717,426,10317,555,110

    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)
    nssv187241801.1e-053273070
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