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nsv6736229

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:65

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 86 SVs from 24 studies. See in: genome view    
    Submitted genomic55,501,366-55,501,430Question Mark
    Overlapping variant regions from other studies: 86 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):56,367,533-56,367,597Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6736229Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr455,501,36655,501,430
    nsv6736229RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr456,367,53356,367,597

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18692192duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18692192Submitted genomicNC_000004.12:g.555
    01366_55501430dup
    GRCh38 (hg38)NC_000004.12Chr455,501,36655,501,430
    nssv18692192RemappedPerfectNC_000004.11:g.563
    67533_56367597dup
    GRCh37.p13First PassNC_000004.11Chr456,367,53356,367,597

    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)
    nssv186921920.0275856215366
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