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nsv6753738

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 181 SVs from 37 studies. See in: genome view    
    Submitted genomic83,457,101-83,462,200Question Mark
    Overlapping variant regions from other studies: 181 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):84,378,254-84,383,353Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6753738Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr483,457,10183,462,200
    nsv6753738RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr484,378,25484,383,353

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18694378duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18694378Submitted genomicNC_000004.12:g.834
    57101_83462200dup
    GRCh38 (hg38)NC_000004.12Chr483,457,10183,462,200
    nssv18694378RemappedPerfectNC_000004.11:g.843
    78254_84383353dup
    GRCh37.p13First PassNC_000004.11Chr484,378,25484,383,353

    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)
    nssv186943784e-061275362
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