nsv6709095

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:110

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 56 SVs from 14 studies. See in: genome view    
    Submitted genomic23,962,834-23,962,943Question Mark
    Overlapping variant regions from other studies: 56 SVs from 14 studies. See in: genome view    
    Remapped(Score: Perfect):24,004,325-24,004,434Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6709095Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr323,962,83423,962,943
    nsv6709095RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr324,004,32524,004,434

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18677491duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18677491Submitted genomicNC_000003.12:g.239
    62834_23962943dup
    GRCh38 (hg38)NC_000003.12Chr323,962,83423,962,943
    nssv18677491RemappedPerfectNC_000003.11:g.240
    04325_24004434dup
    GRCh37.p13First PassNC_000003.11Chr324,004,32524,004,434

    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)
    nssv186774915.2e-0512225274
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