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nsv6986012

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:976

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 138 SVs from 19 studies. See in: genome view    
    Submitted genomic43,030,278-43,031,253Question Mark
    Overlapping variant regions from other studies: 136 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):41,182,295-41,183,270Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6986012Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1743,030,27843,031,253
    nsv6986012RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1741,182,29541,183,270

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18626922duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18626922Submitted genomicNC_000017.11:g.430
    30278_43031253dup
    GRCh38 (hg38)NC_000017.11Chr1743,030,27843,031,253
    nssv18626922RemappedPerfectNC_000017.10:g.411
    82295_41183270dup
    GRCh37.p13First PassNC_000017.10Chr1741,182,29541,183,270

    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)
    nssv186269224e-061256780
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