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nsv6827557

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:383

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 86 SVs from 21 studies. See in: genome view    
    Submitted genomic86,741,112-86,741,494Question Mark
    Overlapping variant regions from other studies: 86 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):86,370,428-86,370,810Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6827557Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr786,741,11286,741,494
    nsv6827557RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr786,370,42886,370,810

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18726148duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18726148Submitted genomicNC_000007.14:g.867
    41112_86741494dup
    GRCh38 (hg38)NC_000007.14Chr786,741,11286,741,494
    nssv18726148RemappedPerfectNC_000007.13:g.863
    70428_86370810dup
    GRCh37.p13First PassNC_000007.13Chr786,370,42886,370,810

    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)
    nssv187261484e-061235000
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