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nsv6651229

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 176 SVs from 38 studies. See in: genome view    
    Submitted genomic54,876,401-54,882,900Question Mark
    Overlapping variant regions from other studies: 176 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):55,342,074-55,348,573Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6651229Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr154,876,40154,882,900
    nsv6651229RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr155,342,07455,348,573

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18630639duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18630639Submitted genomicNC_000001.11:g.548
    76401_54882900dup
    GRCh38 (hg38)NC_000001.11Chr154,876,40154,882,900
    nssv18630639RemappedPerfectNC_000001.10:g.553
    42074_55348573dup
    GRCh37.p13First PassNC_000001.10Chr155,342,07455,348,573

    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)
    nssv186306394e-061273222
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