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nsv6713160

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 94 SVs from 21 studies. See in: genome view    
    Submitted genomic63,944,801-63,947,500Question Mark
    Overlapping variant regions from other studies: 94 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):63,930,477-63,933,176Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6713160Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr363,944,80163,947,500
    nsv6713160RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr363,930,47763,933,176

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18678119duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18678119Submitted genomicNC_000003.12:g.639
    44801_63947500dup
    GRCh38 (hg38)NC_000003.12Chr363,944,80163,947,500
    nssv18678119RemappedPerfectNC_000003.11:g.639
    30477_63933176dup
    GRCh37.p13First PassNC_000003.11Chr363,930,47763,933,176

    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)
    nssv186781192.5e-057271932
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