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nsv6750282

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:586,868

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1763 SVs from 88 studies. See in: genome view    
    Submitted genomic130,633,901-131,220,768Question Mark
    Overlapping variant regions from other studies: 1763 SVs from 88 studies. See in: genome view    
    Remapped(Score: Perfect):131,555,056-132,141,923Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6750282Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4130,633,901131,220,768
    nsv6750282RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4131,555,056132,141,923

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18681927duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18681927Submitted genomicNC_000004.12:g.130
    633901_131220768du
    p
    GRCh38 (hg38)NC_000004.12Chr4130,633,901131,220,768
    nssv18681927RemappedPerfectNC_000004.11:g.131
    555056_132141923du
    p
    GRCh37.p13First PassNC_000004.11Chr4131,555,056132,141,923

    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)
    nssv186819274e-061273840
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