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nsv6961121

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:621,723

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1898 SVs from 82 studies. See in: genome view    
    Submitted genomic55,049,166-55,670,888Question Mark
    Overlapping variant regions from other studies: 1898 SVs from 82 studies. See in: genome view    
    Remapped(Score: Perfect):55,341,364-55,963,086Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6961121Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1555,049,16655,670,888
    nsv6961121RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1555,341,36455,963,086

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18617296duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18617296Submitted genomicNC_000015.10:g.550
    49166_55670888dup
    GRCh38 (hg38)NC_000015.10Chr1555,049,16655,670,888
    nssv18617296RemappedPerfectNC_000015.9:g.5534
    1364_55963086dup
    GRCh37.p13First PassNC_000015.9Chr1555,341,36455,963,086

    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)
    nssv186172964e-061274610
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