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nsv6958289

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:226,252

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 744 SVs from 59 studies. See in: genome view    
    Submitted genomic41,332,755-41,559,006Question Mark
    Overlapping variant regions from other studies: 744 SVs from 59 studies. See in: genome view    
    Remapped(Score: Perfect):41,624,953-41,851,204Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6958289Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1541,332,75541,559,006
    nsv6958289RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1541,624,95341,851,204

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18619366duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18619366Submitted genomicNC_000015.10:g.413
    32755_41559006dup
    GRCh38 (hg38)NC_000015.10Chr1541,332,75541,559,006
    nssv18619366RemappedPerfectNC_000015.9:g.4162
    4953_41851204dup
    GRCh37.p13First PassNC_000015.9Chr1541,624,95341,851,204

    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)
    nssv186193664e-061274854
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