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nsv7010724

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:467,396

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1844 SVs from 84 studies. See in: genome view    
    Submitted genomic5,351,177-5,818,572Question Mark
    Overlapping variant regions from other studies: 1844 SVs from 84 studies. See in: genome view    
    Remapped(Score: Perfect):5,331,823-5,799,218Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7010724Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr205,351,1775,818,572
    nsv7010724RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr205,331,8235,799,218

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18643711duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18643711Submitted genomicNC_000020.11:g.535
    1177_5818572dup
    GRCh38 (hg38)NC_000020.11Chr205,351,1775,818,572
    nssv18643711RemappedPerfectNC_000020.10:g.533
    1823_5799218dup
    GRCh37.p13First PassNC_000020.10Chr205,331,8235,799,218

    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)
    nssv186437114e-061274950
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