nsv6969078

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:291

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 112 SVs from 24 studies. See in: genome view    
    Submitted genomic43,805,193-43,805,483Question Mark
    Overlapping variant regions from other studies: 112 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):44,097,391-44,097,681Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6969078Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1543,805,19343,805,483
    nsv6969078RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1544,097,39144,097,681

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18619492duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18619492Submitted genomicNC_000015.10:g.438
    05193_43805483dup
    GRCh38 (hg38)NC_000015.10Chr1543,805,19343,805,483
    nssv18619492RemappedPerfectNC_000015.9:g.4409
    7391_44097681dup
    GRCh37.p13First PassNC_000015.9Chr1544,097,39144,097,681

    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)
    nssv186194924e-061233874
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