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nsv6647220

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 133 SVs from 37 studies. See in: genome view    
    Submitted genomic20,654,801-20,670,000Question Mark
    Overlapping variant regions from other studies: 133 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):20,981,294-20,996,493Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6647220Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr120,654,80120,670,000
    nsv6647220RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr120,981,29420,996,493

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18609120duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18609120Submitted genomicNC_000001.11:g.206
    54801_20670000dup
    GRCh38 (hg38)NC_000001.11Chr120,654,80120,670,000
    nssv18609120RemappedPerfectNC_000001.10:g.209
    81294_20996493dup
    GRCh37.p13First PassNC_000001.10Chr120,981,29420,996,493

    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)
    nssv186091207e-062274562
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