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nsv6766634

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:663,207

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1834 SVs from 82 studies. See in: genome view    
    Submitted genomic9,181,906-9,845,112Question Mark
    Overlapping variant regions from other studies: 1834 SVs from 82 studies. See in: genome view    
    Remapped(Score: Perfect):9,182,018-9,845,224Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6766634Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr59,181,9069,845,112
    nsv6766634RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr59,182,0189,845,224

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18707119duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18707119Submitted genomicNC_000005.10:g.918
    1906_9845112dup
    GRCh38 (hg38)NC_000005.10Chr59,181,9069,845,112
    nssv18707119RemappedPerfectNC_000005.9:g.9182
    018_9845224dup
    GRCh37.p13First PassNC_000005.9Chr59,182,0189,845,224

    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)
    nssv187071197e-062275664
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