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nsv7017026

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 234 SVs from 18 studies. See in: genome view    
    Submitted genomic5,237,201-5,238,900Question Mark
    Overlapping variant regions from other studies: 234 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):5,237,200-5,238,899Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7017026Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr185,237,2015,238,900
    nsv7017026RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr185,237,2005,238,899

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18634845duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18634845Submitted genomicNC_000018.10:g.523
    7201_5238900dup
    GRCh38 (hg38)NC_000018.10Chr185,237,2015,238,900
    nssv18634845RemappedPerfectNC_000018.9:g.5237
    200_5238899dup
    GRCh37.p13First PassNC_000018.9Chr185,237,2005,238,899

    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)
    nssv186348454e-061262058
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