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nsv6949387

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:402

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 92 SVs from 18 studies. See in: genome view    
    Submitted genomic58,285,414-58,285,815Question Mark
    Overlapping variant regions from other studies: 92 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):58,752,132-58,752,533Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6949387Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1458,285,41458,285,815
    nsv6949387RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1458,752,13258,752,533

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18616392duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18616392Submitted genomicNC_000014.9:g.5828
    5414_58285815dup
    GRCh38 (hg38)NC_000014.9Chr1458,285,41458,285,815
    nssv18616392RemappedPerfectNC_000014.8:g.5875
    2132_58752533dup
    GRCh37.p13First PassNC_000014.8Chr1458,752,13258,752,533

    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)
    nssv186163922.8e-054243318
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