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nsv6709760

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:280,951

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 809 SVs from 56 studies. See in: genome view    
    Submitted genomic58,075,498-58,356,448Question Mark
    Overlapping variant regions from other studies: 809 SVs from 56 studies. See in: genome view    
    Remapped(Score: Perfect):58,061,225-58,342,175Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6709760Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr358,075,49858,356,448
    nsv6709760RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr358,061,22558,342,175

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18677825duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18677825Submitted genomicNC_000003.12:g.580
    75498_58356448dup
    GRCh38 (hg38)NC_000003.12Chr358,075,49858,356,448
    nssv18677825RemappedPerfectNC_000003.11:g.580
    61225_58342175dup
    GRCh37.p13First PassNC_000003.11Chr358,061,22558,342,175

    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)
    nssv186778254e-061273888
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