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nsv6836448

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:349,117

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 759 SVs from 66 studies. See in: genome view    
    Submitted genomic86,851,556-87,200,672Question Mark
    Overlapping variant regions from other studies: 759 SVs from 66 studies. See in: genome view    
    Remapped(Score: Perfect):86,480,872-86,829,988Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6836448Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr786,851,55687,200,672
    nsv6836448RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr786,480,87286,829,988

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18726164duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18726164Submitted genomicNC_000007.14:g.868
    51556_87200672dup
    GRCh38 (hg38)NC_000007.14Chr786,851,55687,200,672
    nssv18726164RemappedPerfectNC_000007.13:g.864
    80872_86829988dup
    GRCh37.p13First PassNC_000007.13Chr786,480,87286,829,988

    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)
    nssv187261644e-061275552
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