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nsv6965069

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:332

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 109 SVs from 21 studies. See in: genome view    
    Submitted genomic59,474,492-59,474,823Question Mark
    Overlapping variant regions from other studies: 109 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):59,766,691-59,767,022Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6965069Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1559,474,49259,474,823
    nsv6965069RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1559,766,69159,767,022

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18620285duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18620285Submitted genomicNC_000015.10:g.594
    74492_59474823dup
    GRCh38 (hg38)NC_000015.10Chr1559,474,49259,474,823
    nssv18620285RemappedPerfectNC_000015.9:g.5976
    6691_59767022dup
    GRCh37.p13First PassNC_000015.9Chr1559,766,69159,767,022

    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)
    nssv186202854e-061241410
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