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nsv6658608

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:35,635

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 258 SVs from 49 studies. See in: genome view    
    Submitted genomic228,413,652-228,449,286Question Mark
    Overlapping variant regions from other studies: 261 SVs from 49 studies. See in: genome view    
    Remapped(Score: Perfect):228,601,353-228,636,987Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6658608Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1228,413,652228,449,286
    nsv6658608RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1228,601,353228,636,987

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18609420duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18609420Submitted genomicNC_000001.11:g.228
    413652_228449286du
    p
    GRCh38 (hg38)NC_000001.11Chr1228,413,652228,449,286
    nssv18609420RemappedPerfectNC_000001.10:g.228
    601353_228636987du
    p
    GRCh37.p13First PassNC_000001.10Chr1228,601,353228,636,987

    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)
    nssv186094204e-061274522
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