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nsv6745901

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:358

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 149 SVs from 45 studies. See in: genome view    
    Submitted genomic114,628,535-114,628,892Question Mark
    Overlapping variant regions from other studies: 149 SVs from 45 studies. See in: genome view    
    Remapped(Score: Perfect):115,549,691-115,550,048Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6745901Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4114,628,535114,628,892
    nsv6745901RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4115,549,691115,550,048

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18682144duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18682144Submitted genomicNC_000004.12:g.114
    628535_114628892du
    p
    GRCh38 (hg38)NC_000004.12Chr4114,628,535114,628,892
    nssv18682144RemappedPerfectNC_000004.11:g.115
    549691_115550048du
    p
    GRCh37.p13First PassNC_000004.11Chr4115,549,691115,550,048

    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)
    nssv186821444e-061229968
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