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nsv6768196

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:64,889

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 304 SVs from 46 studies. See in: genome view    
    Submitted genomic29,331,255-29,396,143Question Mark
    Overlapping variant regions from other studies: 304 SVs from 46 studies. See in: genome view    
    Remapped(Score: Perfect):29,331,362-29,396,250Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6768196Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr529,331,25529,396,143
    nsv6768196RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr529,331,36229,396,250

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18702451duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18702451Submitted genomicNC_000005.10:g.293
    31255_29396143dup
    GRCh38 (hg38)NC_000005.10Chr529,331,25529,396,143
    nssv18702451RemappedPerfectNC_000005.9:g.2933
    1362_29396250dup
    GRCh37.p13First PassNC_000005.9Chr529,331,36229,396,250

    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)
    nssv187024514e-061272014
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