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nsv6908495

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,297

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 89 SVs from 26 studies. See in: genome view    
    Submitted genomic43,479,044-43,482,340Question Mark
    Overlapping variant regions from other studies: 89 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):43,500,594-43,503,890Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6908495Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1143,479,04443,482,340
    nsv6908495RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1143,500,59443,503,890

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18575472duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18575472Submitted genomicNC_000011.10:g.434
    79044_43482340dup
    GRCh38 (hg38)NC_000011.10Chr1143,479,04443,482,340
    nssv18575472RemappedPerfectNC_000011.9:g.4350
    0594_43503890dup
    GRCh37.p13First PassNC_000011.9Chr1143,500,59443,503,890

    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)
    nssv185754724e-061274918
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