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nsv6660725

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:28,246

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 204 SVs from 27 studies. See in: genome view    
    Submitted genomic241,468,061-241,496,306Question Mark
    Overlapping variant regions from other studies: 207 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):241,631,361-241,659,606Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6660725Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1241,468,061241,496,306
    nsv6660725RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1241,631,361241,659,606

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18610100duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18610100Submitted genomicNC_000001.11:g.241
    468061_241496306du
    p
    GRCh38 (hg38)NC_000001.11Chr1241,468,061241,496,306
    nssv18610100RemappedPerfectNC_000001.10:g.241
    631361_241659606du
    p
    GRCh37.p13First PassNC_000001.10Chr1241,631,361241,659,606

    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)
    nssv186101007e-062275748
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