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nsv6719627

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,231

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 85 SVs from 22 studies. See in: genome view    
    Submitted genomic37,957,416-37,961,646Question Mark
    Overlapping variant regions from other studies: 85 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):37,959,037-37,963,267Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6719627Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr437,957,41637,961,646
    nsv6719627RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr437,959,03737,963,267

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18690750duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18690750Submitted genomicNC_000004.12:g.379
    57416_37961646dup
    GRCh38 (hg38)NC_000004.12Chr437,957,41637,961,646
    nssv18690750RemappedPerfectNC_000004.11:g.379
    59037_37963267dup
    GRCh37.p13First PassNC_000004.11Chr437,959,03737,963,267

    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)
    nssv186907501.8e-055274742
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