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nsv6997959

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,865

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 182 SVs from 45 studies. See in: genome view    
    Submitted genomic39,496,105-39,500,969Question Mark
    Overlapping variant regions from other studies: 180 SVs from 45 studies. See in: genome view    
    Remapped(Score: Perfect):37,652,358-37,657,222Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6997959Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1739,496,10539,500,969
    nsv6997959RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1737,652,35837,657,222

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18626750duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18626750Submitted genomicNC_000017.11:g.394
    96105_39500969dup
    GRCh38 (hg38)NC_000017.11Chr1739,496,10539,500,969
    nssv18626750RemappedPerfectNC_000017.10:g.376
    52358_37657222dup
    GRCh37.p13First PassNC_000017.10Chr1737,652,35837,657,222

    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)
    nssv186267507e-062274798
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