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nsv6868418

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:300,745

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 817 SVs from 79 studies. See in: genome view    
    Submitted genomic101,302,335-101,603,079Question Mark
    Overlapping variant regions from other studies: 817 SVs from 79 studies. See in: genome view    
    Remapped(Score: Perfect):104,064,617-104,365,361Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6868418Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9101,302,335101,603,079
    nsv6868418RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9104,064,617104,365,361

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18738909duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18738909Submitted genomicNC_000009.12:g.101
    302335_101603079du
    p
    GRCh38 (hg38)NC_000009.12Chr9101,302,335101,603,079
    nssv18738909RemappedPerfectNC_000009.11:g.104
    064617_104365361du
    p
    GRCh37.p13First PassNC_000009.11Chr9104,064,617104,365,361

    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)
    nssv187389094e-061273906
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