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nsv6877546

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:247,028

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 711 SVs from 62 studies. See in: genome view    
    Submitted genomic35,161,160-35,408,187Question Mark
    Overlapping variant regions from other studies: 718 SVs from 63 studies. See in: genome view    
    Remapped(Score: Perfect):35,161,157-35,408,184Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6877546Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr935,161,16035,408,187
    nsv6877546RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr935,161,15735,408,184

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18749481duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18749481Submitted genomicNC_000009.12:g.351
    61160_35408187dup
    GRCh38 (hg38)NC_000009.12Chr935,161,16035,408,187
    nssv18749481RemappedPerfectNC_000009.11:g.351
    61157_35408184dup
    GRCh37.p13First PassNC_000009.11Chr935,161,15735,408,184

    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)
    nssv187494814e-061273236
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