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nsv6858879

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:277

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 241 SVs from 22 studies. See in: genome view    
    Submitted genomic13,422,595-13,422,871Question Mark
    Overlapping variant regions from other studies: 246 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):13,422,594-13,422,870Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6858879Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr913,422,59513,422,871
    nsv6858879RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr913,422,59413,422,870

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18744043duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18744043Submitted genomicNC_000009.12:g.134
    22595_13422871dup
    GRCh38 (hg38)NC_000009.12Chr913,422,59513,422,871
    nssv18744043RemappedPerfectNC_000009.11:g.134
    22594_13422870dup
    GRCh37.p13First PassNC_000009.11Chr913,422,59413,422,870

    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)
    nssv187440434e-061233212
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