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nsv7004686

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:59,394

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 206 SVs from 35 studies. See in: genome view    
    Submitted genomic51,392,291-51,451,684Question Mark
    Overlapping variant regions from other studies: 206 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):51,895,545-51,954,938Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7004686Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1951,392,29151,451,684
    nsv7004686RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1951,895,54551,954,938

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18638744duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18638744Submitted genomicNC_000019.10:g.513
    92291_51451684dup
    GRCh38 (hg38)NC_000019.10Chr1951,392,29151,451,684
    nssv18638744RemappedPerfectNC_000019.9:g.5189
    5545_51954938dup
    GRCh37.p13First PassNC_000019.9Chr1951,895,54551,954,938

    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)
    nssv186387441.8e-055275374
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