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nsv6725457

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:127

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 101 SVs from 15 studies. See in: genome view    
    Submitted genomic154,373,867-154,373,993Question Mark
    Overlapping variant regions from other studies: 101 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):154,091,656-154,091,782Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6725457Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3154,373,867154,373,993
    nsv6725457RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3154,091,656154,091,782

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18671818duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18671818Submitted genomicNC_000003.12:g.154
    373867_154373993du
    p
    GRCh38 (hg38)NC_000003.12Chr3154,373,867154,373,993
    nssv18671818RemappedPerfectNC_000003.11:g.154
    091656_154091782du
    p
    GRCh37.p13First PassNC_000003.11Chr3154,091,656154,091,782

    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)
    nssv186718184e-061226638
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