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nsv6805135

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:115,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 673 SVs from 70 studies. See in: genome view    
    Submitted genomic17,450,801-17,565,900Question Mark
    Overlapping variant regions from other studies: 673 SVs from 70 studies. See in: genome view    
    Remapped(Score: Perfect):17,490,425-17,605,524Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6805135Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr717,450,80117,565,900
    nsv6805135RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr717,490,42517,605,524

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18724188duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18724188Submitted genomicNC_000007.14:g.174
    50801_17565900dup
    GRCh38 (hg38)NC_000007.14Chr717,450,80117,565,900
    nssv18724188RemappedPerfectNC_000007.13:g.174
    90425_17605524dup
    GRCh37.p13First PassNC_000007.13Chr717,490,42517,605,524

    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)
    nssv187241884e-061273922
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