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nsv6992443

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:495,829

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1646 SVs from 79 studies. See in: genome view    
    Submitted genomic59,074,120-59,569,948Question Mark
    Overlapping variant regions from other studies: 1646 SVs from 79 studies. See in: genome view    
    Remapped(Score: Perfect):57,151,481-57,647,309Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6992443Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1759,074,12059,569,948
    nsv6992443RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1757,151,48157,647,309

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18627316duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18627316Submitted genomicNC_000017.11:g.590
    74120_59569948dup
    GRCh38 (hg38)NC_000017.11Chr1759,074,12059,569,948
    nssv18627316RemappedPerfectNC_000017.10:g.571
    51481_57647309dup
    GRCh37.p13First PassNC_000017.10Chr1757,151,48157,647,309

    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)
    nssv186273164e-061276182
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