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nsv6868235

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

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 111 SVs from 25 studies. See in: genome view    
    Submitted genomic107,012,401-107,013,700Question Mark
    Overlapping variant regions from other studies: 111 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):109,774,682-109,775,981Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6868235Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9107,012,401107,013,700
    nsv6868235RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9109,774,682109,775,981

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18737940duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18737940Submitted genomicNC_000009.12:g.107
    012401_107013700du
    p
    GRCh38 (hg38)NC_000009.12Chr9107,012,401107,013,700
    nssv18737940RemappedPerfectNC_000009.11:g.109
    774682_109775981du
    p
    GRCh37.p13First PassNC_000009.11Chr9109,774,682109,775,981

    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)
    nssv187379400.05614212258204
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