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nsv6759819

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:93,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 411 SVs from 53 studies. See in: genome view    
    Submitted genomic62,355,401-62,449,200Question Mark
    Overlapping variant regions from other studies: 411 SVs from 53 studies. See in: genome view    
    Remapped(Score: Perfect):61,651,228-61,745,027Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6759819Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr562,355,40162,449,200
    nsv6759819RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr561,651,22861,745,027

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18705959duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18705959Submitted genomicNC_000005.10:g.623
    55401_62449200dup
    GRCh38 (hg38)NC_000005.10Chr562,355,40162,449,200
    nssv18705959RemappedPerfectNC_000005.9:g.6165
    1228_61745027dup
    GRCh37.p13First PassNC_000005.9Chr561,651,22861,745,027

    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)
    nssv187059594e-061274180
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