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nsv6650226

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:156,110

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 521 SVs from 64 studies. See in: genome view    
    Submitted genomic43,558,329-43,714,438Question Mark
    Overlapping variant regions from other studies: 521 SVs from 64 studies. See in: genome view    
    Remapped(Score: Perfect):44,024,000-44,180,109Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6650226Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr143,558,32943,714,438
    nsv6650226RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr144,024,00044,180,109

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18628190duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18628190Submitted genomicNC_000001.11:g.435
    58329_43714438dup
    GRCh38 (hg38)NC_000001.11Chr143,558,32943,714,438
    nssv18628190RemappedPerfectNC_000001.10:g.440
    24000_44180109dup
    GRCh37.p13First PassNC_000001.10Chr144,024,00044,180,109

    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)
    nssv186281904e-061275668
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