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nsv6702354

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:98,663

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 376 SVs from 58 studies. See in: genome view    
    Submitted genomic98,003,569-98,102,231Question Mark
    Overlapping variant regions from other studies: 376 SVs from 58 studies. See in: genome view    
    Remapped(Score: Perfect):97,722,413-97,821,075Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6702354Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr398,003,56998,102,231
    nsv6702354RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr397,722,41397,821,075

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18680488duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18680488Submitted genomicNC_000003.12:g.980
    03569_98102231dup
    GRCh38 (hg38)NC_000003.12Chr398,003,56998,102,231
    nssv18680488RemappedPerfectNC_000003.11:g.977
    22413_97821075dup
    GRCh37.p13First PassNC_000003.11Chr397,722,41397,821,075

    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)
    nssv186804887e-062275344
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