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nsv6995316

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,601

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 91 SVs from 23 studies. See in: genome view    
    Submitted genomic50,584,063-50,593,663Question Mark
    Overlapping variant regions from other studies: 91 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):50,617,974-50,627,574Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6995316Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1650,584,06350,593,663
    nsv6995316RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1650,617,97450,627,574

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18624346duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18624346Submitted genomicNC_000016.10:g.505
    84063_50593663dup
    GRCh38 (hg38)NC_000016.10Chr1650,584,06350,593,663
    nssv18624346RemappedPerfectNC_000016.9:g.5061
    7974_50627574dup
    GRCh37.p13First PassNC_000016.9Chr1650,617,97450,627,574

    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)
    nssv186243464e-061275864
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