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nsv7046226

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:706,066

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2406 SVs from 90 studies. See in: genome view    
    Submitted genomic112,507,311-113,213,376Question Mark
    Overlapping variant regions from other studies: 2407 SVs from 90 studies. See in: genome view    
    Remapped(Score: Perfect):113,049,933-113,755,998Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7046226Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1112,507,311113,213,376
    nsv7046226RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1113,049,933113,755,998

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18737044inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18737044Submitted genomicNC_000001.11:g.112
    507311_113213376in
    v
    GRCh38 (hg38)NC_000001.11Chr1112,507,311113,213,376
    nssv18737044RemappedPerfectNC_000001.10:g.113
    049933_113755998in
    v
    GRCh37.p13First PassNC_000001.10Chr1113,049,933113,755,998

    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)
    nssv187370444e-061276268
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