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nsv6968337

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:239

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 67 SVs from 16 studies. See in: genome view    
    Submitted genomic95,290,635-95,290,873Question Mark
    Overlapping variant regions from other studies: 67 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):95,756,972-95,757,210Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6968337Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1495,290,63595,290,873
    nsv6968337RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1495,756,97295,757,210

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18616203duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18616203Submitted genomicNC_000014.9:g.9529
    0635_95290873dup
    GRCh38 (hg38)NC_000014.9Chr1495,290,63595,290,873
    nssv18616203RemappedPerfectNC_000014.8:g.9575
    6972_95757210dup
    GRCh37.p13First PassNC_000014.8Chr1495,756,97295,757,210

    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)
    nssv186162034.1e-0510240658
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