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nsv7039002

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:38

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 121 SVs from 27 studies. See in: genome view    
    Submitted genomic121,526,672-121,526,709Question Mark
    Overlapping variant regions from other studies: 121 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):121,245,519-121,245,556Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7039002Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3121,526,672121,526,709
    nsv7039002RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3121,245,519121,245,556

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18769341inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18769341Submitted genomicNC_000003.12:g.121
    526672_121526709in
    v
    GRCh38 (hg38)NC_000003.12Chr3121,526,672121,526,709
    nssv18769341RemappedPerfectNC_000003.11:g.121
    245519_121245556in
    v
    GRCh37.p13First PassNC_000003.11Chr3121,245,519121,245,556

    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)
    nssv18769341<0.00179273528
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