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nsv6648787

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:223,239

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 580 SVs from 52 studies. See in: genome view    
    Submitted genomic35,688,883-35,912,121Question Mark
    Overlapping variant regions from other studies: 580 SVs from 52 studies. See in: genome view    
    Remapped(Score: Perfect):36,154,484-36,377,722Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6648787Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr135,688,88335,912,121
    nsv6648787RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr136,154,48436,377,722

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18610703duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18610703Submitted genomicNC_000001.11:g.356
    88883_35912121dup
    GRCh38 (hg38)NC_000001.11Chr135,688,88335,912,121
    nssv18610703RemappedPerfectNC_000001.10:g.361
    54484_36377722dup
    GRCh37.p13First PassNC_000001.10Chr136,154,48436,377,722

    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)
    nssv186107034e-061276050
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