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nsv6649171

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,459

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 96 SVs from 26 studies. See in: genome view    
    Submitted genomic34,140,921-34,147,379Question Mark
    Overlapping variant regions from other studies: 96 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):34,606,522-34,612,980Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6649171Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr134,140,92134,147,379
    nsv6649171RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr134,606,52234,612,980

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18610537duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18610537Submitted genomicNC_000001.11:g.341
    40921_34147379dup
    GRCh38 (hg38)NC_000001.11Chr134,140,92134,147,379
    nssv18610537RemappedPerfectNC_000001.10:g.346
    06522_34612980dup
    GRCh37.p13First PassNC_000001.10Chr134,606,52234,612,980

    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)
    nssv186105373.6e-0510274526
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