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nsv7011978

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 84 SVs from 20 studies. See in: genome view    
    Submitted genomic2,732,401-2,734,600Question Mark
    Overlapping variant regions from other studies: 84 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):2,713,047-2,715,246Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7011978Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr202,732,4012,734,600
    nsv7011978RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr202,713,0472,715,246

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18431117deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18431117Submitted genomicNC_000020.11:g.273
    2401_2734600del
    GRCh38 (hg38)NC_000020.11Chr202,732,4012,734,600
    nssv18431117RemappedPerfectNC_000020.10:g.271
    3047_2715246del
    GRCh37.p13First PassNC_000020.10Chr202,713,0472,715,246

    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)
    nssv184311174e-061274506
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