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nsv6947209

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:610,199

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1851 SVs from 95 studies. See in: genome view    
    Submitted genomic42,736,567-43,346,765Question Mark
    Overlapping variant regions from other studies: 1851 SVs from 95 studies. See in: genome view    
    Remapped(Score: Perfect):43,310,703-43,920,901Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6947209Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1342,736,56743,346,765
    nsv6947209RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1343,310,70343,920,901

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18604238duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18604238Submitted genomicNC_000013.11:g.427
    36567_43346765dup
    GRCh38 (hg38)NC_000013.11Chr1342,736,56743,346,765
    nssv18604238RemappedPerfectNC_000013.10:g.433
    10703_43920901dup
    GRCh37.p13First PassNC_000013.10Chr1343,310,70343,920,901

    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)
    nssv186042384e-061275458
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