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nsv6750664

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 135 SVs from 29 studies. See in: genome view    
    Submitted genomic141,696,201-141,700,900Question Mark
    Overlapping variant regions from other studies: 135 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):142,617,354-142,622,053Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6750664Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4141,696,201141,700,900
    nsv6750664RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4142,617,354142,622,053

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18685225duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18685225Submitted genomicNC_000004.12:g.141
    696201_141700900du
    p
    GRCh38 (hg38)NC_000004.12Chr4141,696,201141,700,900
    nssv18685225RemappedPerfectNC_000004.11:g.142
    617354_142622053du
    p
    GRCh37.p13First PassNC_000004.11Chr4142,617,354142,622,053

    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)
    nssv186852254e-061272372
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