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nsv6893994

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:42,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 198 SVs from 32 studies. See in: genome view    
    Submitted genomic106,937,001-106,979,900Question Mark
    Overlapping variant regions from other studies: 198 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):108,696,759-108,739,658Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6893994Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10106,937,001106,979,900
    nsv6893994RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10108,696,759108,739,658

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18580510duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18580510Submitted genomicNC_000010.11:g.106
    937001_106979900du
    p
    GRCh38 (hg38)NC_000010.11Chr10106,937,001106,979,900
    nssv18580510RemappedPerfectNC_000010.10:g.108
    696759_108739658du
    p
    GRCh37.p13First PassNC_000010.10Chr10108,696,759108,739,658

    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)
    nssv185805101.8e-055275152
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