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nsv6711217

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:119,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 329 SVs from 52 studies. See in: genome view    
    Submitted genomic40,479,801-40,598,800Question Mark
    Overlapping variant regions from other studies: 329 SVs from 52 studies. See in: genome view    
    Remapped(Score: Perfect):40,521,292-40,640,291Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6711217Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr340,479,80140,598,800
    nsv6711217RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr340,521,29240,640,291

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18676169duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18676169Submitted genomicNC_000003.12:g.404
    79801_40598800dup
    GRCh38 (hg38)NC_000003.12Chr340,479,80140,598,800
    nssv18676169RemappedPerfectNC_000003.11:g.405
    21292_40640291dup
    GRCh37.p13First PassNC_000003.11Chr340,521,29240,640,291

    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)
    nssv186761691.8e-055273160
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