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nsv6810951

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:19,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 135 SVs from 27 studies. See in: genome view    
    Submitted genomic111,593,501-111,613,300Question Mark
    Overlapping variant regions from other studies: 135 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):111,914,704-111,934,503Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6810951Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6111,593,501111,613,300
    nsv6810951RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6111,914,704111,934,503

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18709486duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18709486Submitted genomicNC_000006.12:g.111
    593501_111613300du
    p
    GRCh38 (hg38)NC_000006.12Chr6111,593,501111,613,300
    nssv18709486RemappedPerfectNC_000006.11:g.111
    914704_111934503du
    p
    GRCh37.p13First PassNC_000006.11Chr6111,914,704111,934,503

    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)
    nssv187094867e-062276074
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