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nsv7006143

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:201,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 958 SVs from 70 studies. See in: genome view    
    Submitted genomic76,068,701-76,270,200Question Mark
    Overlapping variant regions from other studies: 958 SVs from 70 studies. See in: genome view    
    Remapped(Score: Perfect):73,780,656-73,982,155Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7006143Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1876,068,70176,270,200
    nsv7006143RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1873,780,65673,982,155

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18635018duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18635018Submitted genomicNC_000018.10:g.760
    68701_76270200dup
    GRCh38 (hg38)NC_000018.10Chr1876,068,70176,270,200
    nssv18635018RemappedPerfectNC_000018.9:g.7378
    0656_73982155dup
    GRCh37.p13First PassNC_000018.9Chr1873,780,65673,982,155

    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)
    nssv186350184e-061273422
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