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nsv6826128

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:65,737

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 354 SVs from 50 studies. See in: genome view    
    Submitted genomic40,108,338-40,174,074Question Mark
    Overlapping variant regions from other studies: 354 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):40,147,937-40,213,673Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6826128Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr740,108,33840,174,074
    nsv6826128RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr740,147,93740,213,673

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18724144duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18724144Submitted genomicNC_000007.14:g.401
    08338_40174074dup
    GRCh38 (hg38)NC_000007.14Chr740,108,33840,174,074
    nssv18724144RemappedPerfectNC_000007.13:g.401
    47937_40213673dup
    GRCh37.p13First PassNC_000007.13Chr740,147,93740,213,673

    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)
    nssv187241444e-061275158
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