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nsv6719673

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:409,503

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2234 SVs from 83 studies. See in: genome view    
    Submitted genomic39,701,678-40,111,180Question Mark
    Overlapping variant regions from other studies: 2234 SVs from 83 studies. See in: genome view    
    Remapped(Score: Perfect):39,703,298-40,112,800Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6719673Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr439,701,67840,111,180
    nsv6719673RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr439,703,29840,112,800

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18690960duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18690960Submitted genomicNC_000004.12:g.397
    01678_40111180dup
    GRCh38 (hg38)NC_000004.12Chr439,701,67840,111,180
    nssv18690960RemappedPerfectNC_000004.11:g.397
    03298_40112800dup
    GRCh37.p13First PassNC_000004.11Chr439,703,29840,112,800

    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)
    nssv186909604e-061275800
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