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nsv6730279

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,685

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 115 SVs from 33 studies. See in: genome view    
    Submitted genomic130,865,682-130,875,366Question Mark
    Overlapping variant regions from other studies: 115 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):130,584,526-130,594,210Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6730279Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3130,865,682130,875,366
    nsv6730279RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3130,584,526130,594,210

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18671417duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18671417Submitted genomicNC_000003.12:g.130
    865682_130875366du
    p
    GRCh38 (hg38)NC_000003.12Chr3130,865,682130,875,366
    nssv18671417RemappedPerfectNC_000003.11:g.130
    584526_130594210du
    p
    GRCh37.p13First PassNC_000003.11Chr3130,584,526130,594,210

    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)
    nssv186714174e-061273410
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