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nsv7012363

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,850

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 151 SVs from 36 studies. See in: genome view    
    Submitted genomic3,260,766-3,266,615Question Mark
    Overlapping variant regions from other studies: 151 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):3,241,412-3,247,261Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7012363Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr203,260,7663,266,615
    nsv7012363RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr203,241,4123,247,261

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18431580deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18431580Submitted genomicNC_000020.11:g.326
    0766_3266615del
    GRCh38 (hg38)NC_000020.11Chr203,260,7663,266,615
    nssv18431580RemappedPerfectNC_000020.10:g.324
    1412_3247261del
    GRCh37.p13First PassNC_000020.10Chr203,241,4123,247,261

    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)
    nssv184315804e-060276012
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