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nsv7025136

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:448,953

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1391 SVs from 74 studies. See in: genome view    
    Submitted genomic31,456,221-31,905,173Question Mark
    Overlapping variant regions from other studies: 1389 SVs from 74 studies. See in: genome view    
    Remapped(Score: Perfect):30,044,024-30,492,976Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7025136Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2031,456,22131,905,173
    nsv7025136RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2030,044,02430,492,976

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18643520duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18643520Submitted genomicNC_000020.11:g.314
    56221_31905173dup
    GRCh38 (hg38)NC_000020.11Chr2031,456,22131,905,173
    nssv18643520RemappedPerfectNC_000020.10:g.300
    44024_30492976dup
    GRCh37.p13First PassNC_000020.10Chr2030,044,02430,492,976

    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)
    nssv186435204e-061260394
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