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nsv6649163

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,455

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 108 SVs from 27 studies. See in: genome view    
    Submitted genomic33,852,479-33,859,933Question Mark
    Overlapping variant regions from other studies: 108 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):34,318,080-34,325,534Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6649163Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr133,852,47933,859,933
    nsv6649163RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr134,318,08034,325,534

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18610518duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18610518Submitted genomicNC_000001.11:g.338
    52479_33859933dup
    GRCh38 (hg38)NC_000001.11Chr133,852,47933,859,933
    nssv18610518RemappedPerfectNC_000001.10:g.343
    18080_34325534dup
    GRCh37.p13First PassNC_000001.10Chr134,318,08034,325,534

    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)
    nssv186105184e-061275452
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