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nsv6706805

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:28,025

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 153 SVs from 30 studies. See in: genome view    
    Submitted genomic126,481,947-126,509,971Question Mark
    Overlapping variant regions from other studies: 153 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):126,200,790-126,228,814Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6706805Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3126,481,947126,509,971
    nsv6706805RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3126,200,790126,228,814

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18670906duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18670906Submitted genomicNC_000003.12:g.126
    481947_126509971du
    p
    GRCh38 (hg38)NC_000003.12Chr3126,481,947126,509,971
    nssv18670906RemappedPerfectNC_000003.11:g.126
    200790_126228814du
    p
    GRCh37.p13First PassNC_000003.11Chr3126,200,790126,228,814

    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)
    nssv186709061.8e-055274452
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