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nsv6869056

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:396,391

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1717 SVs from 92 studies. See in: genome view    
    Submitted genomic131,228,357-131,624,747Question Mark
    Overlapping variant regions from other studies: 1717 SVs from 92 studies. See in: genome view    
    Remapped(Score: Perfect):134,103,744-134,500,134Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6869056Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9131,228,357131,624,747
    nsv6869056RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9134,103,744134,500,134

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18733152duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18733152Submitted genomicNC_000009.12:g.131
    228357_131624747du
    p
    GRCh38 (hg38)NC_000009.12Chr9131,228,357131,624,747
    nssv18733152RemappedPerfectNC_000009.11:g.134
    103744_134500134du
    p
    GRCh37.p13First PassNC_000009.11Chr9134,103,744134,500,134

    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)
    nssv187331524e-061275804
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