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nsv6971351

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:32,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 208 SVs from 38 studies. See in: genome view    
    Submitted genomic40,865,101-40,897,800Question Mark
    Overlapping variant regions from other studies: 208 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):41,157,299-41,189,998Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6971351Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1540,865,10140,897,800
    nsv6971351RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1541,157,29941,189,998

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18619346duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18619346Submitted genomicNC_000015.10:g.408
    65101_40897800dup
    GRCh38 (hg38)NC_000015.10Chr1540,865,10140,897,800
    nssv18619346RemappedPerfectNC_000015.9:g.4115
    7299_41189998dup
    GRCh37.p13First PassNC_000015.9Chr1541,157,29941,189,998

    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)
    nssv186193467e-062275916
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