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nsv6742326

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,808

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 138 SVs from 30 studies. See in: genome view    
    Submitted genomic141,658,785-141,661,592Question Mark
    Overlapping variant regions from other studies: 138 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):142,579,938-142,582,745Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6742326Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4141,658,785141,661,592
    nsv6742326RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4142,579,938142,582,745

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18488525deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18488525Submitted genomicNC_000004.12:g.141
    658785_141661592de
    l
    GRCh38 (hg38)NC_000004.12Chr4141,658,785141,661,592
    nssv18488525RemappedPerfectNC_000004.11:g.142
    579938_142582745de
    l
    GRCh37.p13First PassNC_000004.11Chr4142,579,938142,582,745

    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)
    nssv184885254e-061275520
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