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nsv6653092

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:147,706

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 463 SVs from 55 studies. See in: genome view    
    Submitted genomic64,907,672-65,055,377Question Mark
    Overlapping variant regions from other studies: 463 SVs from 55 studies. See in: genome view    
    Remapped(Score: Perfect):65,373,355-65,521,060Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6653092Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr164,907,67265,055,377
    nsv6653092RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr165,373,35565,521,060

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18629545duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18629545Submitted genomicNC_000001.11:g.649
    07672_65055377dup
    GRCh38 (hg38)NC_000001.11Chr164,907,67265,055,377
    nssv18629545RemappedPerfectNC_000001.10:g.653
    73355_65521060dup
    GRCh37.p13First PassNC_000001.10Chr165,373,35565,521,060

    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)
    nssv186295454e-061275712
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